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CHILDRENS IBUPROFEN

NDC 30142-281 · KROGER COMPANY

Generic nameIbuprofen
Dosage formSUSPENSION
RouteORAL
Active ingredient(s)IBUPROFEN
Strength100 mg/5mL
Pharmacologic classAnti-Inflammatory Agents, Non-Steroidal [CS], Cyclooxygenase Inhibitors [MoA], Nonsteroidal Anti-inflammatory Drug [EPC]
Marketing categoryANDA

Packages

30142-281-08 — 1 BOTTLE in 1 CARTON (30142-281-08) / 240 mL in 1 BOTTLE

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

27854-777 — Ibuprofen, 29485-6533 — Advil PM, 29485-6552 — IBUPROFEN Capsule, Liquid-filled, 29485-7008 — Advil PM, 29485-9291 — IBUPROFEN 200MG, 30142-050 — diphenhydramine citrate, ibuprofen, 30142-053 — Ibuprofen, 30142-232 — IBUPROFEN, DIPHENHYDRAMINE HCL, 30142-255 — Ibuprofen, 30142-278 — Ibuprofen and Diphenhydramine Citrate, 30142-402 — ibuprofen, 30142-423 — Ibuprofen and Pseudoephedrine Hydrochloride, 30142-497 — Ibuprofen, 30142-513 — ibuprofen, 30142-604 — Ibuprofen, 30142-660 — Ibuprofen, 30142-720 — Acetaminophen, Ibuprofen, 30142-743 — Ibuprofen, 30142-745 — Ibuprofen, 30142-965 — Ibuprofen, +1311 more

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