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
HOMOSALATE; OCTINOXATE; OCTISALATE; OXYBENZONE
Active strength
10; 7.5; 5; 4 mg/100mL; mg/100mL; mg/100mL; mg/100mL
NDC exclude flag
No
Listing certified through
2027-12-31
Current FDA listing
Yes

Additional Listing Data#

Finished product
Yes
Brand name base
Stay Put Sunscreen SPF 30
Listing expiration
2027-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
HOMOSALATE10 mg/100mL
OCTINOXATE7.5 mg/100mL
OCTISALATE5 mg/100mL
OXYBENZONE4 mg/100mL

Harmonized Identifiers#

Field, Values table
FieldValues
UniiV06SV4M95S, 4Y5P7MUD51, 4X49Y0596W, 95OOS7VE0Y

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
70392-020-04Stay Put Sunscreen SPF 30118 mL in 1 BOTTLELOTION1182

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startSampleExclude flagStatus
70392-020-0470392002004118 mL in 1 BOTTLE (70392-020-04) 118 ml2026-03-26NoNoCurrent