Home NDC 68828-021 JAFRA SKIN Glow Face Cream Broad Spectrum SPF 15 Sunscreen
Product NDC 68828-021
11-digit product format 688280021
Labeler code 68828
Product ID 68828-021_2be6020c-f3cd-a932-e063-6394a90a9d73
Type HUMAN OTC DRUG
Nonproprietary name Homosalate, Octisalate, Avobenzone,Octocrylene
Dosage form CREAM
Route TOPICAL
Labeler Distribuidora Comercial Jafra, S.A. de C.V
Application M020
Marketing category OTC MONOGRAPH DRUG
Marketing start 2024-02-14
Substance AVOBENZONE; HOMOSALATE; OCTISALATE; OCTOCRYLENE
Active strength 3; 7; 5; 10 g/100mL; 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 JAFRA SKIN Glow Face Cream Broad Spectrum SPF 15 Sunscreen
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength AVOBENZONE 3 g/100mL HOMOSALATE 7 g/100mL OCTISALATE 5 g/100mL OCTOCRYLENE 10 g/100mL
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 4 matching rows.
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 68828-021-01 JAFRA SKIN Glow Face Cream Broad Spectrum SPF 15 Sunscreen 1 in 1 CARTON CREAM 1 3 68828-021-01 JAFRA SKIN Glow Face Cream Broad Spectrum SPF 15 Sunscreen 30 mL in 1 TUBE CREAM 30 3
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 68828-021 JAFRA SKIN GLOW FACE CREAM BROAD SPECTRUM SPF 15 SUNSCREEN (HOMOSALATE, OCTISALATE, AVOBENZONE,OCTOCRYLENE) CREAM [DISTRIBUIDORA COMERCIAL JAFRA, S.A. DE C.V] 3 Current NDC, 2 package rows 20250119_f627ab5b-85d4-4c92-9412-4bab72828f3d.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 68828-021-01 68828002101 1 TUBE in 1 CARTON (68828-021-01) / 30 mL in 1 TUBE 1 tube 2024-02-14 No No Current