DR LIFT SPF 50 MINERAL SUNSCREEN STICK- zinc oxide stick

Dr Lift SPF 50 Mineral Sunscreen Stick by

Drug Labeling and Warnings

Dr Lift SPF 50 Mineral Sunscreen Stick by is a Otc medication manufactured, distributed, or labeled by Spa de Soleil. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredients

Zinc Oxide 25%

Purpose

Sunscreen

Warnings

Warnings:

For external use only. Do not use on damaged or broken skin.When using this product keep out of eyes. Rinse with water to remove. Stop use and ask a doctor if rash occurs. Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

KEEP OUT OF REACH OF CHILDREN

Keep out of reach of children.

DOSAGE & ADMINISTRATION

Directions: Apply generously and evenly 15 minutes before sun exposure. Ensure complete coverage to the area above the lip, nose, and tops of ears.

INDICATIONS & USAGE

Uses
Provides high protection against sunburn.

Inactive Ingredients

Inactive Ingredients: Caprylic/Capric Triglyceride, Helianthus Annuus (Sunflower) Seed Oil, Prunus Amygdalus Dulcis (Sweet Almond) Oil, Butyrospermum Parkii (Shea) Butter, Cetyl Alcohol, Euphorbia Cerifera (Candelilla) Wax, Helianthus Annuus (Sunflower) Seed Wax, Microcrystalline cellulose, Cocos Nucifera (Coconut) Oil, **Squalane, Tocopheryl Acetate (Vitamin E), Benzyl Alcohol.

Principal Display Panel

INGREDIENTS AND APPEARANCE

DR LIFT SPF 50 MINERAL SUNSCREEN STICK 
zinc oxide stick

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 68062-8314
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC OXIDE - UNII:SOI2LOH54Z)	ZINC OXIDE	3.75 g  in 15 g

Inactive Ingredients
Ingredient Name	Strength
CAPRYLIC/CAPRIC TRIGLYCERIDE (UNII: C9H2L21V7U)
HELIANTHUS ANNUUS SEED WAX (UNII: 42DG15CHXV)
PRUNUS AMYGDALUS DULCIS (SWEET ALMOND) OIL (UNII: 66YXD4DKO9)
BUTYROSPERMUM PARKII (SHEA) BUTTER (UNII: K49155WL9Y)
CETYL ALCOHOL (UNII: 936JST6JCN)
EUPHORBIA CERIFERA (CANDELILLA) WAX (UNII: WL0328HX19)
HELIANTHUS ANNUUS (SUNFLOWER) SEED OIL UNSAPONIFIABLES (UNII: T7ZE2WA4MB)
MICROCRYSTALLINE CELLULOSE (UNII: OP1R32D61U)
COCOS NUCIFERA (COCONUT) OIL (UNII: Q9L0O73W7L)
SQUALANE (UNII: GW89575KF9)
.ALPHA.-TOCOPHEROL ACETATE, D- (UNII: A7E6112E4N)
BENZYL ALCOHOL (UNII: LKG8494WBH)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 68062-8314-1	15 g in 1 TUBE; Type 0: Not a Combination Product	11/12/2025

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M020	11/12/2025

Labeler - Spa de Soleil (874682867)

Establishment
Name	Address	ID/FEI	Business Operations
Spa de Soleil		874682867	manufacture(68062-8314)