FDA.reportPublic FDA data

goPure Sunscreen

Product NDC
83448-025
11-digit product format
834480025
Labeler code
83448
Product ID
83448-025_937c741d-6498-4df3-a385-c4866eb3e8b4
Type
HUMAN OTC DRUG
Nonproprietary name
Zinc oxide
Dosage form
LOTION
Route
TOPICAL
Labeler
Natural Lifestyle Brands, LLC dba GoPure beauty
Application
M020
Marketing category
OTC MONOGRAPH DRUG
Marketing start
2023-08-28
Substance
ZINC OXIDE
Active strength
25 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
goPure Sunscreen
Listing expiration
2026-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
ZINC OXIDE25 g/100mL

Harmonized Identifiers#

Field, Values table
FieldValues
UniiSOI2LOH54Z

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
83448-025-15goPure Sunscreen1 in 1 CARTONLOTION14
83448-025-15goPure Sunscreen15 mL in 1 TUBELOTION154
83448-025-50goPure Sunscreen1 in 1 CARTONLOTION14
83448-025-50goPure Sunscreen50 mL in 1 TUBELOTION504

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
83448-025GOPURE SUNSCREEN (ZINC OXIDE) LOTION [NATURAL LIFESTYLE BRANDS, LLC DBA GOPURE BEAUTY]3Current NDC, 4 package rows20241226_a74ec20b-8436-4030-820c-01fd88134f40.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startSampleExclude flagStatus
83448-025-15834480025151 TUBE in 1 CARTON (83448-025-15) / 15 mL in 1 TUBE1 tube2024-02-16NoNoHistorical
83448-025-50834480025501 TUBE in 1 CARTON (83448-025-50) / 50 mL in 1 TUBE1 tube2023-08-28NoNoHistorical