DR LIFT SPF 50 CLEAR STICK- avobenzone, homosalate, octisalate, octocrylene stick

Dr Lift SPF 50 Clear Stick by

Drug Labeling and Warnings

Dr Lift SPF 50 Clear 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

Butyl Methoxydibenzoylmethane 3.0%

Ethylhexyl Salicylate 5.0%

Homosalate 10.0%

Octocrylene 10.0%

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: C12-15 Alkyl Benzoate, Ethylhexyl Palmitate, Polyamide-8, Polyamide-3, Isostearyl Isostearate, Butyloctyl Salicylate, Ethylhexyl Methoxycrylene, Polyester-8, BHT, Pentaerythrityl Tetra-di-t-butyl Hydroxyhydrocinnamate, Tocopheryl Acetate (Vitamin E).

Principal Display Panel

INGREDIENTS AND APPEARANCE

DR LIFT SPF 50 CLEAR STICK 
avobenzone, homosalate, octisalate, octocrylene stick

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 68062-8313
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
OCTISALATE (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W)	OCTISALATE	0.74 mg  in 14.8 mL
OCTOCRYLENE (UNII: 5A68WGF6WM) (OCTOCRYLENE - UNII:5A68WGF6WM)	OCTOCRYLENE	1.48 mg  in 14.8 mL
AVOBENZONE (UNII: G63QQF2NOX) (AVOBENZONE - UNII:G63QQF2NOX)	AVOBENZONE	0.4 mg  in 14.8 mL
HOMOSALATE (UNII: V06SV4M95S) (HOMOSALATE - UNII:V06SV4M95S)	HOMOSALATE	1.48 mg  in 14.8 mL

Inactive Ingredients
Ingredient Name	Strength
C12-15 ALKYL BENZOATE (UNII: A9EJ3J61HQ)
ETHYLHEXYL PALMITATE (UNII: 2865993309)
POLYAMIDE-8 (4500 MW) (UNII: 77723GV81A)
POLYAMIDE-3 (20000 MW) (UNII: PLF06VZ9SQ)
ISOSTEARYL ISOSTEARATE (UNII: IV0Z586Z4Y)
BUTYLOCTYL SALICYLATE (UNII: 2EH13UN8D3)
ETHYLHEXYL METHOXYCRYLENE (UNII: S3KFG6Q5X8)
POLYESTER-8 (1400 MW, CYANODIPHENYLPROPENOYL CAPPED) (UNII: T9296U138P)
BHT (UNII: 1P9D0Z171K)
PENTAERYTHRITYL TETRA-DI-T-BUTYL HYDROXYHYDROCINNAMATE (UNII: 255PIF62MS)
.ALPHA.-TOCOPHEROL ACETATE, D- (UNII: A7E6112E4N)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 68062-8313-1	14.8 mL in 1 TUBE; Type 0: Not a Combination Product	10/09/2025

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M020	10/09/2025

Labeler - Spa de Soleil (874682867)

Establishment
Name	Address	ID/FEI	Business Operations
Spa de Soleil		874682867	manufacture(68062-8313)