# Public Health, Seattle and King County — Hazardous Materials Safety Interpretation

- **operation:** document
- **citation:** 10-0153
- **title:** Public Health, Seattle and King County — Hazardous Materials Safety Interpretation
- **source type:** guidance
- **agency:** Pipeline and Hazardous Materials Safety Administration
- **status:** guidance
- **official:** true
- **published on:** 2010-12-08
- **effective on:** Not available
- **summary:** 10-0153 response to Public Health, Seattle and King County concerning 171.8, 172.101, 173.21.
- **machine formats:** - **json:** https://regulus.evalyn.ai/document/phmsa-interpretation-10-0153.json
- **markdown:** https://regulus.evalyn.ai/document/phmsa-interpretation-10-0153.md
- **app url:** https://regulus.evalyn.ai/document/phmsa-interpretation-10-0153
- **source url:** https://www.phmsa.dot.gov/sites/phmsa.dot.gov/files/legacy/interpretations/Interpretations/2010/100153.pdf
**body:**

<<<PAGE 1>>>

U.S. Department of Transportation 1200 New Jersey Ave. SE
Washington, D.C. 20590
Pipeline and Hazardous Materials
Safety Administration
r:: 0 820m
Mr. William Perry
Health and Environmental Investigator II
Public Health, Seattle and King County
401 Fifth Avenue, Suite 1100
Seattle, WA 98104
Reference No. 10-0153
Dear Mr. Perry:
This is in response to your telephone conversation with a member of my staff, and your
subsequent e-mail and attachments requesting clarification of the Hazardous Materials
Regulations (HMR; 49 CFR Parts 171-180) applicable to waste pharmaceuticals. Specifically,
you present two transportation plans pertaining to a pilot program the City of Seattle and King
County, Washington, would like to begin in these communities to collect waste pharmaceuticals
from consumers and transport them for disposal by common carriers using motor vehicles. You
described the plans for collecting these materials and conditions common to both, and ask if a
special permit or competent authority approval is needed to transport these materials on a onetime
or long-term operational basis. You also ask how long it would take to obtain this type of
permission. We have paraphrased your questions and answered them in the order you provided.
You state conditions common to the pharmaceuticals in both scenarios are these materials are:
1) Drug Enforcement Administration Schedule 2-5 controlled substances; 2) household
hazardous waste exempt under the Environmental Protection Agency's Resource Conservation
and Recovery Act and Washington State Dangerous Waste Regulations; and 3) unwanted
medications delivered by residents to approved drop-off locations or collected by law
enforcement offices in Snohomish County, W A.
Before packing, you state: 1) all the materials collected will be reviewed by a pharmacist
experienced at screening returned medicines and sorted by this pharmacist into controlled and
non-controlled categories; 2) unacceptable items under the program's criteria will be removed
(e.g., sharps, liquid mercury, aerosol cans, etc.); 3) non-controlled medicines will be packaged by
a permitted hazardous waste disposal vendor; and 4) controlled medicines will be packaged in a
4 milliliter thick plastic drum liner that is closed with a zip-tie and placed in a 10 or 15 gallon,
UN 1 G standard fiber drum. You also state full packages will be sealed with tamper-evident
tape, tracked and shipped by a common carrier from the Bothell, W A, Police Department to the
Sauget, IL, Police Department, and disposed of using an approved method, such as incineration.

<<<PAGE 2>>>

You provided one photograph of typical medicines collected, one photograph of a completed
package, and two website links that contain examples of the fiber drum packaging.
Scenario A
Medicines will be left in their original consumer packagings. As items containing liquids are
packed, the integrity and tightness of their lids will be checked and corrected as needed. Liquid
containers will be packed upright and pill vial packagings will be used to separate the liquid
containers from each other and the sides ofthe fiber drum. By weight, an estimate of the
contents, based on inventories of materials collected from another pilot program (PH:ARM), is
66 percent will be medications and 34 percent will be packaging materials and containers, and 70
percent ofthe medicines will be solids and 30 percent will be liquids. The materials packed
according to Scenario A will be marked and labeled as "Consumer commodity, ORM-D." This
completed package will weigh 66 pounds or less.
Scenario B
Solid medicines will be removed from their original packagings and transferred into an approved
outer packaging. Liquids and ointments will remain in their original consumer packagings. As
items containing liquids are packed, the integrity and tightness of their lids will be checked and
corrected as needed. Liquid containers will be packed upright and loose pills will be used to
separate the liquid containers from each other and the sides of the fiber drum. Additional
commercial absorbent (e.g., kitty litter) will be used as needed to provide protective cushioning
and absorb any leaked liquid contents. By weight, an estimate ofthe contents, based on
inventories of materials collected from another pilot program (PH:ARM), is 90 percent of the
contents will be solids, and 10 percent will be liquids or ointments and their containers. The
materials packed according to this scenario will be marked, labeled, and described as "UN 3249,
Medicine, solid, toxic, n.o.s., 6.1 (poisonous), Packing Group (PG) II" or "UN 1851, Medicine,
liquid, toxic, n.o.s., 6.1, Packing Group (PG) II." This completed package will weigh
approximately 60 pounds.
Based on the information you submitted, the materials packaged as described in both scenarios
are permitted in transportation under the HMR provided these materials are compatible with the
packaging materials and do not react dangerously with each other (see §§ 173.21, 173.24,
173.24a, and 173.153). Completed packages that contain liquids must be marked with
directional arrows to indicate the correct (upright) orientation ofthese inner packagings and their
closures within the outer packaging (see § 172.312(a)(2)). Also, please note materials prepared
in conformance with Scenario B must have the technical name entered in parentheses as a part of
the proper shipping description on a shipping paper either after the proper shipping name or at
the end ofthe basic description (see § 172.203(k)). As defined in § 171.8 of the HMR,
"technical name" means a recognized chemical name or microbiological name currently used in
scientific and technical handbooks, journals, and texts. A generic description may be used as a
technical name for a Division 6.1 material provided it readily identifies the general chemical
group.

<<<PAGE 3>>>

If the packaging and accompanying materials do not meet the criteria prescribed in the HMR, the
packaging will have to be approved under the terms of a special permit. The application process
is described in 49 CFR Part 107, Subpart B. Processing times for the issuance of a special permit
vary based on the complexity and completeness of the application, but this agency requests that
the application be submitted at least 120 days before the requested date the applicant want the
special permit becomes effective. For a special permit to be issued, the Pipeline and Hazardous
Materials Safety Administration must find that the procedure the applicant has requested
maintains a level of safety at least equal to the level required under the HMR.
I hope this satisfies your request.
Sincerely,
---/(~
~~
~x~~~a15l-r-~~-,-------
T. Glenn Foster
Chief, Regulatory Review and Reinvention
Standards and Rulemaking Division

<<<PAGE 4>>>

Edmonson
§ 17Z~ ;0/
Edmonson. Eileen (PHMSA)
From: Perry, William [William.Perry@kingcounty.gov]
Sent: Monday, June 14, 20106:04 PM
To: Edmonson, Eileen (PHMSA)
Cc: Grasso, Cheri
Subject: Details of Shipment of Waste Medicines - WA State Pilot
Attachments: Packaging Description_WP _06142010.doc
Greetings, Eileen I'm
following up on our conversation of a couple of weeks ago regarding the shipment of pharmaceutical materials via
common carrier. I've attached a description of the pilot project that we've cooked up here, now with two scenarios.
«Packaging Description_WP_06142010.doc»
From our conversation, it sounds like our procedures and packaging generally meet DOT's criteria for safe shipment of
this material. My questions to you now would be For
this one time demonstration, are their any speCial approvals from DOT that would be required?
If this were being done on an operational basis, would it require a special permit? If so, how long would that take.?
Thanks for your help with this issue - the complexity of the DOT regulations and website make it especially nice to
communicate with a real person Tata-
Will
Will Perry
Health & Environmental Investigator II
Public Health I Seattle & King County
401 Fifth Ave, Suite 1100
Seattle, W A 98104
206-263-8477 william.perry@kingconnty.gov
1

<<<PAGE 5>>>

OUTLINE FOR THE SHIPMENT OF CONTROLLED SUBSTANCES TO
HAZARDOUS WASTE INCINERATION Will Perry 6·14-2010
POINTS COMMON TO SCENARIO A OR B
Material used in this pilot will be unwanted medications from residents, collected by the law
enforcement offices in Snohomish County, Washington.
All materials will be HHW exempt by RCRA and WA State Dangerous Waste Regulations
criteria.
Contents will be Controlled Substances listed as Schedule 2 5 drugs by the Drug Enforcement
Administration.
Before packing, all materials will be screened by a pharmacist that is experienced at screening
returned medicines. This screening will remove sharps, liquid mercury, aerosol cans or any
other materials that are not acceptable under the program criteria. The pharmacist will sort the
collected medicines into controlled and non-controlled categories. Non-controlled medicines
will be packed for pickup by a permitted hazardous waste disposal vendor.
The controlled substance medications identified by the pharmacist will be packaged for shipment
via common carrier. Outer packaging will be a 10 or 15 gallon 10 fiber drums. Exampleshttp://www.ulinc.comlProductlDetail/S·l
07 56/Drums-And-Pails/l a-Gallon -Fiber-Drum
http://www.graingcr.comiGrai nger/items/2PYK 7? Pid=scarcll
A 4-mil plastic drum liner will be used, and closed with a zip-tie before the fiber drum is closed.
Full packages will be sealed using tamper-evident tape, and then shipped by common carrier
(UPS or FedEx) from the Bothell, W A Police Department to the Sauget, IL Police Department.
Throughout the shipment, the custody and location of the package will be tracked and
documented using the carrier's procedures.
SCENARIO A
Medicines will be left in their original consumer packaging. As liquid containers are packed, the
integrity & tightness of the lids will be checked and corrected as needed. Liquid containers will
be packed upright, with pill vials providing separation from other liquid containers and the sides
of the fiber drum.
By weight, an estimated 66% of the contents will be medications - and estimated 34 % will be
packaging and containers.
By weight, an estimated 70% of the medicines will be solids (e. g., pills, patches)
By weight, an estimated 30% of the medicines will be liquids (e. g., narcotic cough syrups)
Estimates are based on inventories of collected material from the PH:ARM pilot.
The drum will be shipped and labeled as aRM-D.

<<<PAGE 6>>>

SCENARIOB
Solid medicines will be removed from their original packaging and poured into an approved
outer package. Liquids & ointments will be left in their original consumer packaging. As liquid
containers are packed, the integrity & tightness of the lids will be checked and corrected as
needed. Liquid containers will be packed upright, with the loose pills providing separation from
other containers and the sides of the fiber drum. Additional commercial absorbent ("kitty litter")
will be used as needed to provide protective cushioning.
By weight, an estimated 90% of the contents will be solids (e. g., pills, patches)
By weight, an estimated 10% of the contents will be liquids or ointments (e. g., narcotic cough
syrups) and their containers
Estimates are based on inventories of collected material from the PH:ARM pilot.
The drum will be shipped and labeled as Medicine, solid, toxic, n.o.s.; Packing Group II. and
Medicine, liquid, toxic, n.o.s., Packing Group II.
In the interest of convenient handling, the sealed package will weigh around 60 pounds.
If there are questions or items for discussion, please contact Will
Perry
Health & Environmental Investigator II
Public Health / Seattle & King County
401 Fifth Ave, Suite 1100
Seattle, WA 98104
206-263-8477 william.perry@kingcounty.gov
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