(RE) Setting 100% Mineral Powder Medium Broad Spectrum Sunscreen SPF 35

Product NDC
75936-167
11-digit product format
759360167
Labeler code
75936
Product ID
75936-167_47f8a2f2-05c0-3c88-e063-6294a90ab92a
Type
HUMAN OTC DRUG
Nonproprietary name
Zinc Oxide
Dosage form
POWDER
Route
TOPICAL
Labeler
Supergoop, LLC
Application
M020
Marketing category
OTC MONOGRAPH DRUG
Marketing start
2020-09-08
Substance
ZINC OXIDE
Active strength
24.7 g/100g
NDC exclude flag
No
Listing certified through
2027-12-31
Current FDA listing
Yes

Additional Listing Data#

Finished product
Yes
Brand name base
(RE) Setting 100% Mineral Powder Medium Broad Spectrum Sunscreen SPF 35
Listing expiration
2027-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
ZINC OXIDE24.7 g/100g

Harmonized Identifiers#

Field, Values table
FieldValues
UniiSOI2LOH54Z

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
75936-167-01(RE) Setting 100% Mineral Powder Medium Broad Spectrum Sunscreen SPF 354.25 g in 1 BOTTLEPOWDER4.256
75936-167-02(RE) Setting 100% Mineral Powder Medium Broad Spectrum Sunscreen SPF 354.25 g in 1 JARPOWDER4.256

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
75936-167(RE) SETTING 100% MINERAL POWDER MEDIUM BROAD SPECTRUM SUNSCREEN SPF 35 (ZINC OXIDE) POWDER [SUPERGOOP, LLC]5Current NDC, Legacy NDC, 2 package rows20241208_af4b0f17-43ec-a176-e053-2a95a90a7ac6.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
75936-167-01759360167014.25 g in 1 BOTTLE (75936-167-01) 4.25 g2020-09-080000-00-00NoNoCurrent
75936-167-02759360167024.25 g in 1 JAR (75936-167-02) 4.25 g2020-09-080000-00-00NoNoCurrent