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Minoxidil

NDC 84382-001 · Clarity Cosmetics Inc.

Generic nameMinoxidil Foam 5% (Womens)
Dosage formAEROSOL, FOAM
RouteTOPICAL
Active ingredient(s)MINOXIDIL
Strength50 mg/g
Pharmacologic classArteriolar Vasodilation [PE], Arteriolar Vasodilator [EPC]
Marketing categoryANDA

Packages

84382-001-04 — 1 CAN in 1 PACKAGE (84382-001-04) / 60 g in 1 CAN

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

84232-012 — Mens foam Minoxidil 1 pk, 84232-014 — Mens foam Minoxidil 6 pk, 84232-016 — Womens foam Minoxidil 1 pk, 84232-018 — Womens foam Minoxidil 6 pk, 84232-021 — Male Liquid Minoxidil (6pk) Derma Roller Included, 84329-465 — MINOXIDIL, 84329-466 — MINOXIDIL, 84355-003 — Minoxidil, 84355-004 — Minoxidil, 84355-005 — MINOXIDIL, 84454-001 — Minoxidil, 84539-001 — MINOXIDIL, 84539-002 — FINASTERIDE FOAM WITH 5% MINOXIDIL, 84558-011 — Ollm 5% MINOXIDIL Growth Serum, 84561-514 — MINOXIDIL, 84561-524 — MINOXIDIL, 84614-001 — Minoxidil, 84614-003 — Minoxidil, 84856-603 — MINOXIDIL, 84856-604 — MINOXIDIL, +292 more

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