Home NDC 69842-022 SkinPharmacy Advanced Anti-Aging Therapy Retinol Day Moisturizer SPF 30
Product NDC 69842-022
11-digit product format 698420022
Labeler code 69842
Product ID 69842-022_60a54a3a-98ed-4ece-999a-75df89236947
Type HUMAN OTC DRUG
Nonproprietary name homosalate, octisalate, avobenzone, octocrylene, oxybenzone
Dosage form LIQUID
Route TOPICAL
Labeler CVS Health
Application part352
Marketing category OTC MONOGRAPH NOT FINAL
Marketing start 2014-10-01
Substance AVOBENZONE; HOMOSALATE; OCTISALATE; OCTOCRYLENE; OXYBENZONE
Active strength 20; 100; 50; 15; 40 mg/mL; mg/mL; mg/mL; mg/mL; mg/mL
NDC exclude flag No
Listing certified through 2026-12-31
Current FDA listing Yes Additional Listing Data#
Finished product Yes
Brand name base SkinPharmacy Advanced Anti-Aging Therapy Retinol Day Moisturizer SPF 30
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength HOMOSALATE 20 mg/mL OCTISALATE 100 mg/mL AVOBENZONE 50 mg/mL OCTOCRYLENE 15 mg/mL OXYBENZONE 40 mg/mL
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 5 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 69842-022-01 SkinPharmacy Advanced Anti-Aging Therapy Retinol Day Moisturizer SPF 30 1 in 1 CARTON LIQUID 1 1 69842-022-01 SkinPharmacy Advanced Anti-Aging Therapy Retinol Day Moisturizer SPF 30 30 mL in 1 TUBE LIQUID 30 1
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 69842-022 SKINPHARMACY ADVANCED ANTI-AGING THERAPY RETINOL DAY MOISTURIZER SPF 30 (HOMOSALATE, OCTISALATE, AVOBENZONE, OCTOCRYLENE, OXYBENZONE) LIQUID [CVS HEALTH] 1 Current NDC, Legacy NDC, 2 package rows 20170329_17cd30b6-55c8-423e-a7f8-e4ef2329422e.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 1 of 1 · 1 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 69842-022-01 69842002201 1 TUBE in 1 CARTON (69842-022-01) / 30 mL in 1 TUBE 1 tube 2014-10-01 0000-00-00 No No Current