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Midol Complete Caffeine Free

NDC 0280-0078 · Bayer HealthCare LLC.

Generic nameACETAMINOPHEN, CAFFEINE, and PYRILAMINE MALEATE
Dosage formTABLET
RouteORAL
Active ingredient(s)ACETAMINOPHEN, PAMABROM, PYRILAMINE MALEATE
Strength500; 25; 15 mg/1; mg/1; mg/1
Marketing categoryOTC MONOGRAPH DRUG

Packages

0280-0078-01 — 6 BLISTER PACK in 1 CARTON (0280-0078-01) / 4 TABLET in 1 BLISTER PACK

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

0143-9386 — Acetaminophen, 0143-9432 — ACETAMINOPHEN and IBUPROFEN, 0245-0410 — Hydrocodone Bitartrate and Acetaminophen, 0245-0411 — Hydrocodone Bitartrate and Acetaminophen, 0245-0412 — Hydrocodone Bitartrate and Acetaminophen, 0264-4050 — Acetaminophen, 0264-4100 — Acetaminophen, 0280-0055 — chlorpheniramine maleate, dextromethorphan hydrobromide, acetaminophen, phenylephrine hydrochloride, 0280-0061 — acetaminophen, dextromethorphan hydrobromide, guaifenesin, phenylephrine hydrochloride, 0280-0070 — pamabrom, 0280-0088 — chlorpheniramine maleate, acetaminophen, phenylephrine hydrochloride, dextromethorphan hydrobromide, 0280-0092 — Acetaminophen, Chlorpheniramine malaeate, Dextromethorphan hydrobromide, Phenylephrine hydrochloride, 0280-0095 — Acetaminophen, Dextromethorphan hydrobromide , Phenylephrine hydrochloride, 0280-0097 — Acetaminophen, Dextromethorphan hydrobromide , Doxylamine Succinate, Phenylephrine hydrochloride, 0280-0151 — chlorpheniramine maleate, acetaminophen, dextromethorphan hydrobromide, 0280-0152 — acetaminophen, dextromethorphan hydrobromide, 0280-0505 — Alka-Seltzer Plus Severe Cough Mucus and Congestion, 0280-0507 — Acetaminophen, Dextromethorphan hydrobromide, Guaifenesin, Phenylephrine hydrochloride, 0280-0921 — ACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE, GUAIFENESIN, and PHENYLEPHRINE HYDROCHLORIDE, 0280-0922 — ACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE, DOXYLAMINE SUCCINATE, and PHENYLEPHRINE HYDROCHLORIDE, +3500 more

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