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e l f Camo Semi Matte CC SPF 30 Light 280 N

NDC 76354-515 · e.l.f. Cosmetics, Inc.

Generic nameZINC OXIDE, TITANIUM DIOXIDE, HOMOSALATE, OCTISALATE, OCTOCRYLENE
Dosage formCREAM
RouteTOPICAL
Active ingredient(s)ZINC OXIDE, TITANIUM DIOXIDE, HOMOSALATE, OCTISALATE, OCTOCRYLENE
Strength50; 45; 30; 60; 63 mg/g; mg/g; mg/g; mg/g; mg/g
Pharmacologic classCopper Absorption Inhibitor [EPC], Decreased Copper Ion Absorption [PE]
Marketing categoryOTC MONOGRAPH DRUG

Packages

76354-515-01 — 1 TUBE in 1 CARTON (76354-515-01) / 30 g in 1 TUBE

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

76354-483 — ZINC OXIDE, 76354-490 — ZINC OXIDE, 76354-491 — ZINC OXIDE, 76354-492 — ZINC OXIDE, 76354-493 — ZINC OXIDE, 76354-510 — ZINC OXIDE, TITANIUM DIOXIDE, HOMOSALATE, OCTISALATE, OCTOCRYLENE, 76354-511 — ZINC OXIDE, TITANIUM DIOXIDE, HOMOSALATE, OCTISALATE, OCTOCRYLENE, 76354-512 — ZINC OXIDE, TITANIUM DIOXIDE, HOMOSALATE, OCTISALATE, OCTOCRYLENE, 76354-513 — ZINC OXIDE, TITANIUM DIOXIDE, HOMOSALATE, OCTISALATE, OCTOCRYLENE, 76354-514 — ZINC OXIDE, TITANIUM DIOXIDE, HOMOSALATE, OCTISALATE, OCTOCRYLENE, 76354-516 — ZINC OXIDE, TITANIUM DIOXIDE, HOMOSALATE, OCTISALATE, OCTOCRYLENE, 76354-517 — ZINC OXIDE, TITANIUM DIOXIDE, HOMOSALATE, OCTISALATE, OCTOCRYLENE, 76354-518 — ZINC OXIDE, TITANIUM DIOXIDE, HOMOSALATE, OCTISALATE, OCTOCRYLENE, 76354-519 — ZINC OXIDE, TITANIUM DIOXIDE, HOMOSALATE, OCTISALATE, OCTOCRYLENE, 76354-520 — ZINC OXIDE, TITANIUM DIOXIDE, HOMOSALATE, OCTISALATE, OCTOCRYLENE, 76354-521 — ZINC OXIDE, TITANIUM DIOXIDE, HOMOSALATE, OCTISALATE, OCTOCRYLENE, 76354-522 — ZINC OXIDE, TITANIUM DIOXIDE, HOMOSALATE, OCTISALATE, OCTOCRYLENE, 76354-523 — ZINC OXIDE, TITANIUM DIOXIDE, HOMOSALATE, OCTISALATE, OCTOCRYLENE, 76354-524 — ZINC OXIDE, TITANIUM DIOXIDE, HOMOSALATE, OCTISALATE, OCTOCRYLENE, 76354-525 — ZINC OXIDE, TITANIUM DIOXIDE, HOMOSALATE, OCTISALATE, OCTOCRYLENE, +8384 more

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