UNSPSC 51162302: Acetaminophen/aluminum acetate/chlorpheniramine/phenylpropanolam
Commodity
Code facts
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UNSPSC codes and definitions come from the UN Development Programme (managed by GS1 US), and state and local contract opportunities from the governments' procurement sites.
NIGP codes for 51162302
Definition
This classification denotes a combination drug defined by the U.S. Department of Veterans Affairs in its (VA's) National Drug File (NDF), which falls under VA Drug Class RE599. This VA Drug Class (RE599) classifies this compound as belonging to the group COLD REMEDIES, OTHER.
The first component of this combination drug is an analgesic and antipyretic with the molecular formula C8H9NO2, a preparation that US FDA recognizes as an active ingredient or moiety under Unique Ingredient Identifier 362O9ITL9D, chemically known as n-(4-hydroxyphenyl)acetamide but more generally known as acetaminophen, which bears U.S. National Institutes of Health Compound Identifier 1983. Acetaminophen comes in many forms, including base, acetate, cysteine, cysteinylglycine, di-methyl derivative, glucuronide, glutathione, hemisuccinate, mercapturate, and sulfate.
Read the full definition
The European Medicines Agency schedules Acetaminophen in its eXtended EudraVigilance Medicinal Product Dictionary or XEVMPD under Index SUB09611MIG. The World Health Organization schedules acetaminophen in its Anatomical Therapeutic Chemical (ATC) Classification. The second component of this combination drug is an astringent, a preparation that US FDA recognizes as an active ingredient or moiety under Unique Ingredient Identifier 80EHD8I43D. The European Medicines Agency schedules Aluminium acetate in its eXtended EudraVigilance Medicinal Product Dictionary or XEVMPD under Index SUB12809MIG.
Aluminum acetate generally arises in the molecular formula 3C2H3O2.AL. The term 'aluminum acetate' is a U.S. Pharmacopeial Convention designation. The third component of this combination drug is a histamine-1 receptor antagonist, a preparation that US FDA recognizes as an active ingredient or moiety under Unique Ingredient Identifier 3U6IO1965U. The European Medicines Agency schedules chlorphenamine (in maleate form, the most common form) in its eXtended EudraVigilance Medicinal Product Dictionary or XEVMPD under Index SUB01243MIG.
Chlorpheniramine generally arises in the molecular formula C16H19ClN2. The term 'chlorpheniramine' is a European Pharmacopoeia designation. The fourth component of this combination drug is an adrenergic agonist with the molecular formula C9H13NO, a preparation that US FDA recognizes as an active ingredient or moiety under Unique Ingredient Identifier 33RU150WUN, chemically known as 1r,2s-(-)-norephedrine but more generally known as phenylpropanolamine, which bears U.S. National Institutes of Health Compound Identifier 4786.
The European Medicines Agency schedules Phenylpropanolamine in its eXtended EudraVigilance Medicinal Product Dictionary or XEVMPD under Index SUB09790MIG. The term PHENYLPROPANOLAMINE is an International Non-Proprietary Name or INN (see World Health Organization INN reference publication, Volume 3, No. 3, 1989, List 29). The World Health Organization schedules phenylpropanolamine in its Anatomical Therapeutic Chemical (ATC) Classification.
About UNSPSC 51162302
UNSPSC 51162302 Acetaminophen/aluminum acetate/chlorpheniramine/phenylpropanolam is a Commodity code under which state and local governments procure pharmaceutical products and medical supplies, though recent opportunities show divergence from the code's nominal scope. The Washington State Department of Corrections (DOC) solicitation RFQQK13020 for parenteral products, services, and equipment targets intravenous solutions, parenteral nutrition (TPN and PPN), and controlled substances for incarcerated individuals across eight correctional facilities, with delivery requirements of 24 hours for PN bags and 8 hours for other parenteral products. A separate Seminole County, Florida procurement (IFB60459723LAS) sought naloxone and drug deactivation systems for community health initiatives. The issuing bodies include state departments of corrections and county health authorities, reflecting the code's application to institutional healthcare procurement rather than retail pharmacy or consumer pharmaceutical distribution.
Recent activity concentrates in Washington state and Florida, with the Washington DOC procurement representing the more substantial engagement—DOC anticipates selecting up to three contractors per region across West, Central, and East zones, with an initial contract term running November 26, 2026 through June 30, 2030 and fixed pricing for the first two years. The Washington DOC RFQ closed October 7, 2026, and included set-aside aspirations (small business 25%, minority-owned 10%, women-owned 6%, veteran-owned 5%) under Chapter 39.19 RCW. Contractors must maintain Commercial General Liability ($1 million per occurrence / $2 million aggregate), Professional Liability ($2 million per occurrence / aggregate), Business Automobile Liability ($1 million per occurrence / $2 million aggregate), and Cyber Liability ($2 million per occurrence / aggregate). The Seminole County opportunity, posted June 30, 2026 with a due date of July 26, 2023, appears to contain a date inconsistency in the source and specified annual volumes of 1,900 units of naloxone and 800 drug deactivation systems with quarterly deliveries. Overall, the code shows limited recent activity and significant scope divergence from its pharmaceutical product name, warranting verification that opportunities are being tagged to the correct commodity classification.
Quick answers
What is UNSPSC 51162302?
UNSPSC 51162302 is Acetaminophen/
Which NIGP codes match UNSPSC 51162302?
UNSPSC 51162302 maps to 1 NIGP code, 26948 Expectorants, Antitussives, and Mucolytic Agents.
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