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LOreal Paris Infallible ProGlow Broad Spectrum SPF 15 Sunscreen

NDC 49967-043 · L'Oreal USA Products Inc

Generic nameOctinoxate
Dosage formLIQUID
RouteTOPICAL
Active ingredient(s)OCTINOXATE
Strength32 mg/mL
Marketing categoryOTC MONOGRAPH DRUG

Packages

49967-043-02 — 30 mL in 1 TUBE (49967-043-02)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

49527-081 — AVOBENZONE, OCTINOXATE, OCTISALATE, and OXYBENZONE, 49527-083 — AVOBENZONE,HOMOSALATE,OCTINOXATE,OCTISALATE, 49527-084 — AVOBENZONE,HOMOSALATE,OCTINOXATE,OCTISALATE, 49527-118 — Octinoxate, Titanium Dioxide, 49527-220 — ENSULIZOLE, OCTINOXATE, OCTISALATE, and ZINC OXIDE, 49825-138 — Avobenzone, Octinoxate, Octisalate, Octocrylene, Oxybenzone, 49825-201 — Avobenzone, Homosalate, Octinoxate, Octisalate, Octocrylene, Oxybenzone, 49967-007 — Octinoxate, 49967-009 — Octinoxate and Titanium Dioxide, 49967-015 — Homosalate, Meradimate, Octinoxate, Zinc Oxide, and Octocrylene, 49967-132 — Octinoxate, 49967-180 — Octinoxate and Titanium Dioxide, 49967-196 — Octinoxate, 49967-202 — Octinoxate, 49967-270 — Octinoxate and Titanium Dioxide, 49967-302 — Octinoxate and Titanium dioxide, 49967-303 — Octinoxate and Titanium dioxide, 49967-335 — Octinoxate and Titanium Dioxide, 49967-346 — Homosalate, Octinoxate, Octisalate, Octocrylene and Zinc Oxide, 49967-439 — Octinoxate, +1648 more

From the FDA National Drug Code Directory, retrieved 2026-08-24. Product listings are submitted by labelers; FDA does not verify them.