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Tretinoin

NDC 68682-513 · Oceanside Pharmaceuticals

Generic nameTretinoin
Dosage formGEL
RouteTOPICAL
Active ingredient(s)TRETINOIN
Strength1 mg/g
Pharmacologic classRetinoid [EPC], Retinoids [CS]
Marketing categoryNDA AUTHORIZED GENERIC

Packages

68682-513-82 — 1 TUBE in 1 CARTON (68682-513-82) / 20 g in 1 TUBE

68682-513-84 — 1 TUBE in 1 CARTON (68682-513-84) / 45 g in 1 TUBE

68682-513-85 — 1 BOTTLE, PUMP in 1 CARTON (68682-513-85) / 50 g in 1 BOTTLE, PUMP

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

68071-3825 — tretinoin, 68071-3826 — tretinoin, 68071-3865 — tretinoin, 68071-3888 — tretinoin, 68071-3889 — Tretinoin, 68071-3945 — tretinoin, 68084-075 — Tretinoin, 68308-777 — tretinoin, 68462-792 — Tretinoin, 68682-300 — clindamycin phosphate and tretinoin, 68682-514 — Tretinoin, 68682-515 — Tretinoin, 68682-800 — Tretinoin, 68788-4069 — tretinoin, 68788-8857 — tretinoin, 69238-2323 — Tretinoin, 70518-3233 — tretinoin, 70771-1873 — Tretinoin, 71335-2898 — Tretinoin, 71335-2952 — Tretinoin, +70 more

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