Dr Lift Mineral SPF 50

Product NDC
68062-8311
11-digit product format
680628311
Labeler code
68062
Product ID
68062-8311_40c04b10-2eb5-3a52-e063-6394a90ad407
Type
HUMAN OTC DRUG
Nonproprietary name
titanium dioxide, zinc oxide
Dosage form
SPRAY
Route
TOPICAL
Labeler
Spa de Soleil
Application
M020
Marketing category
OTC MONOGRAPH DRUG
Marketing start
2025-10-09
Substance
TITANIUM DIOXIDE; ZINC OXIDE
Active strength
72; 952 mg/100mL; mg/100mL
NDC exclude flag
No
Listing certified through
2026-12-31
Current FDA listing
Yes

Additional Listing Data#

Finished product
Yes
Brand name base
Dr Lift Mineral SPF 50
Listing expiration
2026-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
TITANIUM DIOXIDE72 mg/100mL
ZINC OXIDE952 mg/100mL

Harmonized Identifiers#

Field, Values table
FieldValues
Unii15FIX9V2JP, SOI2LOH54Z

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
68062-8311-1Dr Lift Mineral SPF 50100 mL in 1 BOTTLE, SPRAYSPRAY1001

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startSampleExclude flagStatus
68062-8311-168062831101100 mL in 1 BOTTLE, SPRAY (68062-8311-1) 100 ml2025-10-09NoNoCurrent