SUN and SHINE MINERAL SUNSCREEN

Product NDC
69435-1505
11-digit product format
694351505
Labeler code
69435
Product ID
69435-1505_48300ffa-cb1a-1829-e063-6294a90a3054
Type
HUMAN OTC DRUG
Nonproprietary name
ZINC OXIDE
Dosage form
CREAM
Route
TOPICAL
Labeler
Peer Pharm Ltd.
Application
M020
Marketing category
OTC MONOGRAPH DRUG
Marketing start
2022-05-19
Substance
ZINC OXIDE
Active strength
24.5 g/100mL
NDC exclude flag
No
Listing certified through
2027-12-31
Current FDA listing
Yes

Additional Listing Data#

Finished product
Yes
Brand name base
SUN and SHINE MINERAL SUNSCREEN
Listing expiration
2027-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
ZINC OXIDE24.5 g/100mL

Harmonized Identifiers#

Field, Values table
FieldValues
UniiSOI2LOH54Z

FDA-Initiated Inactive NDC Indexing#

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
69435-1505-1SUN and SHINE MINERAL SUNSCREEN1 in 1 CARTONCREAM13
69435-1505-1SUN and SHINE MINERAL SUNSCREEN50 mL in 1 TUBECREAM503

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
69435-1505SUN AND SHINE MINERAL SUNSCREEN (ZINC OXIDE) CREAM [PEER PHARM LTD.]2Current NDC, Legacy NDC, 2 package rows20240220_897eb75c-d7d6-4fce-afdd-f794fd8a82fd.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
69435-1505-1694351505011 TUBE in 1 CARTON (69435-1505-1) / 50 mL in 1 TUBE1 tube2022-05-190000-00-00NoNoCurrent