Home NDC 68828-802 Always Liquid Foundation Makeup Sunscreen Broad Spectrum SPF 15 - Golden Tan
Product NDC 68828-802
11-digit product format 688280802
Labeler code 68828
Product ID 68828-802_41ac8e3b-2838-6667-e063-6394a90a291e
Type HUMAN OTC DRUG
Nonproprietary name Homosalate, Octisalate, Zinc Oxide
Dosage form LIQUID
Route TOPICAL
Labeler Distribuidora Comercial Jafra, S.A. de C.V.
Application M020
Marketing category OTC MONOGRAPH DRUG
Marketing start 2024-01-18
Substance OCTISALATE; ZINC OXIDE; HOMOSALATE
Active strength 4.75; 6.75; 4.25 g/100mL; g/100mL; g/100mL
NDC exclude flag No
Listing certified through 2026-12-31
Current FDA listing Yes Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.
Additional Listing Data#
Finished product Yes
Brand name base Always Liquid Foundation Makeup Sunscreen Broad Spectrum SPF 15 - Golden Tan
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength OCTISALATE 4.75 g/100mL ZINC OXIDE 6.75 g/100mL HOMOSALATE 4.25 g/100mL
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 3 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 4X49Y0596W Internal UNII lookup SOI2LOH54Z Internal UNII lookup V06SV4M95S Internal UNII lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 68828-802-01 Always Liquid Foundation Makeup Sunscreen Broad Spectrum SPF 15 - Golden Tan 30 mL in 1 TUBE LIQUID 30 3 68828-802-01 Always Liquid Foundation Makeup Sunscreen Broad Spectrum SPF 15 - Golden Tan 1 in 1 CARTON LIQUID 1 3
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 68828-802 ALWAYS LIQUID FOUNDATION MAKEUP SUNSCREEN BROAD SPECTRUM SPF 15 - GOLDEN TAN (HOMOSALATE, OCTISALATE, ZINC OXIDE) LIQUID [DISTRIBUIDORA COMERCIAL JAFRA, S.A. DE C.V.] 2 Current NDC, 2 package rows 20241129_7f4a185c-85c7-43bf-8695-c01a3aecec0d.zip
openFDA label cross-check# OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.
Matched openFDA labels page 128 of 357 · 7,139 matching rows.
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Sample Exclude flag Status 68828-802-01 68828080201 1 TUBE in 1 CARTON (68828-802-01) / 30 mL in 1 TUBE 1 tube 2024-01-18 No No Current