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Extra Strength Headache, Circle K

NDC 66715-5506 · Lil' Drug Store Products, Inc.

Generic nameacetaminophen/aspirin/caffeine tablet
Dosage formTABLET
RouteORAL
Active ingredient(s)ASPIRIN, CAFFEINE, ACETAMINOPHEN
Strength250; 250; 65 mg/1; mg/1; mg/1
Pharmacologic classAnti-Inflammatory Agents, Non-Steroidal [CS], Central Nervous System Stimulant [EPC], Central Nervous System Stimulation [PE], Cyclooxygenase Inhibitors [MoA], Decreased Platelet Aggregation [PE], Decreased Prostaglandin Production [PE], Methylxanthine [EPC], Nonsteroidal Anti-inflammatory Drug [EPC], Platelet Aggregation Inhibitor [EPC], Xanthines [CS]
Marketing categoryOTC MONOGRAPH DRUG

Packages

66715-5506-4 — 1 BOTTLE, PLASTIC in 1 CARTON (66715-5506-4) / 50 TABLET in 1 BOTTLE, PLASTIC

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

65145-157 — Acetaminophen, 65162-033 — Acetaminophen and Codeine, 65162-115 — Hydrocodone Bitartrate and Acetaminophen, 65162-207 — Oxycodone and Acetaminophen, 65162-596 — Aspirin and Extended-Release Dipyridamole, 65862-922 — Tramadol Hydrochloride and Acetaminophen, 66267-319 — Hydrocodone Bitartrate and Acetaminophen, 66715-5206 — buffered aspirin, 66715-5438 — Acetaminophen, Caffeine, Aspirin tablet, 66715-5504 — Aspirin, 66715-5531 — Acetaminophen, Dextromethorphan Hydrobromide, and Phenylephrine Hydrochloride, 66715-5533 — Acetaminophen, 66715-5534 — Acetaminophen, Dextromethorphan Hydrobromide, and Doxylamine Succinate, 66715-5544 — Acetaminophen, Guaifenesin, Phenylephrine HCl caplet, film-coated, 66715-5571 — Acetaminophen, Dextromethorphan Hydrobromide, and PHENYLEPHRINE HYDROCHLORIDE, 66715-5572 — Acetaminophen, Dextromethorphan Hydrobromide, and Doxylamine Succinate, 66715-5628 — Acetaminophen, Dextromethorphan HBr, Phenylephrine HCI tablet, film-coated, 66715-5632 — Acetaminophen, Guaifenesin, Phenylephrine HCl caplet, film-coated, 66715-5635 — acetaminophen tablet, film coated, 66715-5640 — acetaminophen, diphenhydramine hcl tablet, film coated, +4118 more

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