Sunscreen Cream

Product NDC
84938-012
11-digit product format
849380012
Labeler code
84938
Product ID
84938-012_46224dbe-a0fc-c242-e063-6394a90a2634
Type
HUMAN OTC DRUG
Nonproprietary name
Zinc Oxide 15%,Titanium Dioxide 6%,Homosalate 5%,Octisalate 4%
Dosage form
CREAM
Route
TOPICAL
Labeler
Foshan Sugar Max Cosmetics CO.,Ltd
Application
M020
Marketing category
OTC MONOGRAPH DRUG
Marketing start
2025-12-17
Substance
HOMOSALATE; OCTISALATE; TITANIUM DIOXIDE; ZINC OXIDE
Active strength
.05; .04; .06; .15 g/mL; g/mL; g/mL; g/mL
NDC exclude flag
No
Listing certified through
2026-12-31
Current FDA listing
Yes

Additional Listing Data#

Finished product
Yes
Brand name base
Sunscreen Cream
Listing expiration
2026-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
HOMOSALATE.05 g/mL
OCTISALATE.04 g/mL
TITANIUM DIOXIDE.06 g/mL
ZINC OXIDE.15 g/mL

Harmonized Identifiers#

Field, Values table
FieldValues
UniiV06SV4M95S, 4X49Y0596W, 15FIX9V2JP, SOI2LOH54Z

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
84938-012-01Sunscreen Cream90 mL in 1 BOTTLECREAM901

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startSampleExclude flagStatus
84938-012-018493800120190 mL in 1 BOTTLE (84938-012-01) 90 ml2025-12-17NoNoCurrent