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ZEUS

NDC 84697-001 · NEWPORT APOTHECARY, INC

Generic nameZINC OXIDE
Dosage formCREAM
RouteTOPICAL
Active ingredient(s)ZINC OXIDE
Strength22.3 g/100mL
Pharmacologic classCopper Absorption Inhibitor [EPC], Decreased Copper Ion Absorption [PE]
Marketing categoryOTC MONOGRAPH DRUG

Packages

84697-001-01 — 1 BOTTLE in 1 CARTON (84697-001-01) / 50 mL in 1 BOTTLE

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

84632-0503 — Zinc Oxide, 84632-3031 — Non- Nano Zinc Oxide, 84632-3032 — Zinc Oxide, 84632-3056 — Zinc Oxide, 84632-3057 — Zinc Oxide, 84632-3058 — Zinc Oxide, 84632-3059 — Non- Nano Zinc Oxide, 84656-530 — ZINC OXIDE, 84662-030 — Zinc Oxide, 84662-060 — Zinc Oxide, Homosalate, Octocrylene, 84722-3036 — ZINC OXIDE, 84722-3078 — DIMETHICONE, 84723-001 — Zinc Oxide, 84723-006 — ZINC OXIDE, 84723-007 — Zinc Oxide, 84747-530 — ZINC OXIDE, 84749-001 — Zinc Oxide, 84755-0001 — Krx Aesthetics All Day Glow Sunblocker, 84755-0003 — Clinical Skin Filter Tinted Sunscreen, 84755-0004 — Clinical Skin Filter Tinted Sunscreen Medium Dark, +4478 more

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