Home NDC 68479-020 Powerbright Moisturizer SPF 50
Product NDC 68479-020
11-digit product format 684790020
Labeler code 68479
Product ID 68479-020_bf9d0db0-b478-475f-aeb0-9a8ddd643ac2
Type HUMAN OTC DRUG
Nonproprietary name Octocrylene, Homosalate, Avobenzone, and Octisalate
Dosage form LOTION
Route TOPICAL
Labeler Dermalogica, LLC.
Application M020
Marketing category OTC MONOGRAPH DRUG
Marketing start 2021-03-04
Substance OCTOCRYLENE; HOMOSALATE; AVOBENZONE; OCTISALATE
Active strength 80; 50; 30; 30 mg/mL; mg/mL; mg/mL; mg/mL
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 Powerbright Moisturizer SPF 50
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength OCTOCRYLENE 80 mg/mL HOMOSALATE 50 mg/mL AVOBENZONE 30 mg/mL OCTISALATE 30 mg/mL
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 Product Concepts# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 68479-020-01 Powerbright Moisturizer SPF 50 12 mL in 1 TUBE LOTION 12 2 68479-020-02 Powerbright Moisturizer SPF 50 50 mL in 1 BOTTLE LOTION 50 2 68479-020-02 Powerbright Moisturizer SPF 50 1 in 1 CARTON LOTION 1 2 68479-020-05 Powerbright Moisturizer SPF 50 7 mL in 1 TUBE LOTION 7 2 68479-020-06 Powerbright Moisturizer SPF 50 2 mL in 1 POUCH LOTION 2 2
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 68479-020 POWERBRIGHT MOISTURIZER SPF 50 (OCTOCRYLENE, HOMOSALATE, AVOBENZONE, AND OCTISALATE) LOTION [DERMALOGICA, LLC.] 2 Current NDC, Legacy NDC, 5 package rows 20250101_02c731ee-c5cb-4158-9b1f-e826593c3526.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 26 of 357 · 7,139 matching rows.
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Marketing end Sample Exclude flag Status 68479-020-01 68479002001 12 mL in 1 TUBE (68479-020-01) 12 ml 2021-03-04 0000-00-00 No No Current 68479-020-02 68479002002 1 BOTTLE in 1 CARTON (68479-020-02) / 50 mL in 1 BOTTLE 1 bottle 2021-03-04 0000-00-00 No No Current 68479-020-05 68479002005 7 mL in 1 TUBE (68479-020-05) 7 ml 2021-03-04 0000-00-00 No No Current 68479-020-06 68479002006 2 mL in 1 POUCH (68479-020-06) 2 ml 2021-03-04 0000-00-00 No No Current