Skip to main content

Tylenol PM

NDC 50580-608 · Kenvue Brands LLC

Generic nameacetaminophen and diphenhydramine hydrochloride
Dosage formTABLET, FILM COATED
RouteORAL
Active ingredient(s)ACETAMINOPHEN, DIPHENHYDRAMINE HYDROCHLORIDE
Strength500; 25 mg/1; mg/1
Pharmacologic classHistamine H1 Receptor Antagonists [MoA], Histamine-1 Receptor Antagonist [EPC]
Marketing categoryOTC MONOGRAPH DRUG

Packages

50580-608-01 1 BOTTLE in 1 CARTON (50580-608-01) / 24 TABLET, FILM COATED in 1 BOTTLE

50580-608-02 1 BOTTLE in 1 CARTON (50580-608-02) / 100 TABLET, FILM COATED in 1 BOTTLE

50580-608-03 1 BOTTLE in 1 CARTON (50580-608-03) / 150 TABLET, FILM COATED in 1 BOTTLE

50580-608-04 1 BOTTLE in 1 CARTON (50580-608-04) / 225 TABLET, FILM COATED in 1 BOTTLE

50580-608-05 2 TABLET, FILM COATED in 1 POUCH (50580-608-05)

50580-608-06 50 POUCH in 1 TRAY (50580-608-06) / 2 TABLET, FILM COATED in 1 POUCH

50580-608-07 2 POUCH in 1 CARTON (50580-608-07) / 2 TABLET, FILM COATED in 1 POUCH

50580-608-08 1 BOTTLE in 1 CARTON (50580-608-08) / 50 TABLET, FILM COATED in 1 BOTTLE

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

50580-566 — Acetaminophen, Guaifenesin, and Phenylephrine Hydrochloride, 50580-573 — Diphenhydramine hydrochloride, 50580-575 — Acetaminophen, 50580-576 — acetaminophen, 50580-579 — Acetaminophen, 50580-584 — Acetaminophen, Guaifenesin, 50580-586 — Acetaminophen and Dextromethorphan Hydrobromide, 50580-590 — acetaminophen, 50580-598 — Acetaminophen and Phenylephrine hydrochloride, 50580-599 — acetaminophen, 50580-612 — Acetaminophen, 50580-614 — ACETAMINOPHEN, 50580-659 — Acetaminophen, Pseudoephedrine, 50580-692 — acetaminophen, 50580-783 — Acetaminophen, 50580-843 — diphenhydramine hydrochloride, 50580-937 — Acetaminophen, 50594-863 — Acetaminophen, Diphenhydramine HCL, 50804-048 — Allergy Relief, 50804-064 — Diphenhydramine HCl, Zinc Acetate, +4329 more

From the FDA National Drug Code Directory, retrieved August 24, 2026. Product listings are submitted by labelers; FDA does not verify them.

Read from: FDA National Drug Code Directory, product.txt and package.txt (accessdata.fda.gov/cder/ndctext.zip) — Snapshot retrieved 2026-08-24, loaded 2026-08-24; CMS Medicare Part B Drug Average Sales Price (ASP) Pricing Files (cms.gov/medicare/payment/part-b-drugs/asp-pricing-files) -- the NDC-HCPCS crosswalk and Part B payment limit files — 2026 Q3 (July 2026 release). All data sources · How to read the labels