Mineral Sunscreen Lip

Product NDC
85372-212
11-digit product format
853720212
Labeler code
85372
Product ID
85372-212_4627750c-bc7d-ce6e-e063-6394a90ae28b
Type
HUMAN OTC DRUG
Nonproprietary name
Titanium Dioxide, Zinc Oxide
Dosage form
STICK
Route
TOPICAL
Labeler
Glow Advanced Skin and Body Care, LLC
Application
M020
Marketing category
OTC MONOGRAPH DRUG
Marketing start
2022-05-13
Substance
TITANIUM DIOXIDE; ZINC OXIDE
Active strength
40; 55 mg/g; mg/g
NDC exclude flag
No
Listing certified through
2026-12-31
Current FDA listing
Yes

Additional Listing Data#

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

Active Ingredients#

Ingredient, Strength table
IngredientStrength
TITANIUM DIOXIDE40 mg/g
ZINC OXIDE55 mg/g

Harmonized Identifiers#

Field, Values table
FieldValues
Unii15FIX9V2JP, SOI2LOH54Z

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
c5cd4727-ac49-4409-82b1-5bd8006c3ec7Product name120171122

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
85372-212-45Mineral Sunscreen Lip4.5 g in 1 CYLINDERSTICK4.52
85372-212-45Mineral Sunscreen Lip1 in 1 CARTONSTICK12

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startSampleExclude flagStatus
85372-212-45853720212451 CYLINDER in 1 CARTON (85372-212-45) / 4.5 g in 1 CYLINDER1 cylinder2022-05-13NoNoHistorical