SPF50 Sunscreen

Product NDC
73928-010
11-digit product format
739280010
Labeler code
73928
Product ID
73928-010_40979dfb-f669-17bd-e063-6394a90ac717
Type
HUMAN OTC DRUG
Nonproprietary name
Sunscreen
Dosage form
CREAM
Route
TOPICAL
Labeler
KINGKEY MBC LIFE TECHNOLOGY GROUP CO., LTD
Application
M020
Marketing category
OTC MONOGRAPH DRUG
Marketing start
2020-11-10
Substance
HOMOSALATE; OCTOCRYLENE; OXYBENZONE; TITANIUM DIOXIDE; ZINC OXIDE
Active strength
10; 9.8; 2; 8; 3 g/100mL; g/100mL; g/100mL; g/100mL; g/100mL
NDC exclude flag
No
Listing certified through
2026-12-31
Current FDA listing
Yes

Additional Listing Data#

Finished product
Yes
Brand name base
SPF50 Sunscreen
Listing expiration
2026-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
HOMOSALATE10 g/100mL
OCTOCRYLENE9.8 g/100mL
OXYBENZONE2 g/100mL
TITANIUM DIOXIDE8 g/100mL
ZINC OXIDE3 g/100mL

Harmonized Identifiers#

Field, Values table
FieldValues
UniiV06SV4M95S, 5A68WGF6WM, 95OOS7VE0Y, 15FIX9V2JP, SOI2LOH54Z

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
73928-010-01SPF50 Sunscreen80 mL in 1 TUBECREAM804

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
73928-010SPF50 SUNSCREEN (SUNSCREEN) CREAM [KINGKEY MBC LIFE TECHNOLOGY GROUP CO., LTD]3Current NDC, Legacy NDC, 1 package rows20241120_b3cde609-7d62-2ac7-e053-2a95a90a26b3.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
73928-010-017392800100180 mL in 1 TUBE (73928-010-01) 80 ml2020-11-100000-00-00NoNoCurrent