Home NDC 70392-020 Stay Put Sunscreen SPF 30
Product NDC 70392-020
11-digit product format 703920020
Labeler code 70392
Product ID 70392-020_4e0242e2-28ba-8c42-e063-6294a90a7d01
Type HUMAN OTC DRUG
Nonproprietary name Octinoxate 7.50% Octisalate 5.00% Oxybenzone 4.00% Homosalate 10.00%
Dosage form LOTION
Route TOPICAL
Labeler Sawyer Products Inc
Application M020
Marketing category OTC MONOGRAPH DRUG
Marketing start 2026-03-26
Substance OCTINOXATE; OCTISALATE; OXYBENZONE; HOMOSALATE
Active strength 7.5; 5; 4; 10 mg/100mL; mg/100mL; mg/100mL; mg/100mL
NDC exclude flag No
Listing certified through 2027-12-31
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 Stay Put Sunscreen SPF 30
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength OCTINOXATE 7.5 mg/100mL OCTISALATE 5 mg/100mL OXYBENZONE 4 mg/100mL HOMOSALATE 10 mg/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 70392-020-04 Stay Put Sunscreen SPF 30 118 mL in 1 BOTTLE LOTION 118 2
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 Sample Exclude flag Status 70392-020-04 70392002004 118 mL in 1 BOTTLE (70392-020-04) 118 ml 2026-03-26 No No Current