Home NDC 68828-801 Always Liquid Foundation Makeup Sunscreen Broad Spectrum SPF 15 - Natural Tan
Product NDC 68828-801
11-digit product format 688280801
Labeler code 68828
Product ID 68828-801_41ac9cab-fb80-8ded-e063-6394a90a9493
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 ZINC OXIDE; HOMOSALATE; OCTISALATE
Active strength 6.75; 4.25; 4.75 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 - Natural Tan
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength ZINC OXIDE 6.75 g/100mL HOMOSALATE 4.25 g/100mL OCTISALATE 4.75 g/100mL
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 3 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination SOI2LOH54Z Internal UNII lookup V06SV4M95S Internal UNII lookup 4X49Y0596W 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 68828-801-01 Always Liquid Foundation Makeup Sunscreen Broad Spectrum SPF 15 - Natural Tan 30 mL in 1 TUBE LIQUID 30 3 68828-801-01 Always Liquid Foundation Makeup Sunscreen Broad Spectrum SPF 15 - Natural 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 68828-801 ALWAYS LIQUID FOUNDATION MAKEUP SUNSCREEN BROAD SPECTRUM SPF 15 - NATURAL TAN (HOMOSALATE, OCTISALATE, ZINC OXIDE) LIQUID [DISTRIBUIDORA COMERCIAL JAFRA, S.A. DE C.V] 2 Current NDC, 2 package rows 20241129_3617d26e-a94c-4665-988b-95dbbc527017.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 27 of 354 · 7,077 matching rows.
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Sample Exclude flag Status 68828-801-01 68828080101 1 TUBE in 1 CARTON (68828-801-01) / 30 mL in 1 TUBE 1 tube 2024-01-18 No No Current