GARNIER ULTRA LIFT SPF 30 DEEP WRINKLE DAY- avobenzone, homosalate, octisalate and octocrylene cream

Garnier Ultra Lift SPF 30 Deep Wrinkle Day by

Drug Labeling and Warnings

Garnier Ultra Lift SPF 30 Deep Wrinkle Day by is a Otc medication manufactured, distributed, or labeled by L'Oreal USA Products Inc. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active ingredients

Avobenzone 3%, Homosalate 2%, Octisalate 5%, Octocrylene 7%

Warnings

For external use only. 

When using this product

keep out of eyes. Rinse with water to remove.

Stop use and consult a doctor if 

rash or irritation develops and lasts.

Keep out of reach of children.

f swallowed, get medical help or contact a Poison Control Center right away.

Directions

Apply before sun exposure

Inactive ingredients

water, glycerin, dimethicone, aluminum starch octenylsuccinate, glyceryl stearate SE, polyglyceryl-3 methylglucose distearate, stearyl alcohol, ammonium polyacryloyldimethyl taurate, argania spinosa kernel extract, benzyl alcohol, caprylyl glycol, carbomer, disodium EDTAS, disodium stearoyl glutamate, hydrolyzed rice protein, linalool, maltodextrin, manilkara multinervis leaf extract, methylparaben, palmitic acid, pentaerythrityl tetra-di-t-butyl hydroxyhydrocinnamate, phenoxyethanol, retinyl linoleate, sodium cocoyl glutamate, stearic acid, xanthan gum, fragrance

Uses

Helps prevent sunburn. Higher SPF gives more sunburn protection.

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

GARNIER ULTRA LIFT SPF 30 DEEP WRINKLE DAY 
avobenzone, homosalate, octisalate and octocrylene cream

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 49967-092
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
Avobenzone (UNII: G63QQF2NOX) (Avobenzone - UNII:G63QQF2NOX)	Avobenzone	30 mg  in 1 mL
Homosalate (UNII: V06SV4M95S) (Homosalate - UNII:V06SV4M95S)	Homosalate	20 mg  in 1 mL
Octisalate (UNII: 4X49Y0596W) (Octisalate - UNII:4X49Y0596W)	Octisalate	50 mg  in 1 mL
Octocrylene (UNII: 5A68WGF6WM) (Octocrylene - UNII:5A68WGF6WM)	Octocrylene	70 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
GLYCERIN (UNII: PDC6A3C0OX)
DIMETHICONE (UNII: 92RU3N3Y1O)
ALUMINUM STARCH OCTENYLSUCCINATE (UNII: I9PJ0O6294)
GLYCERYL STEARATE SE (UNII: FCZ5MH785I)
STEARYL ALCOHOL (UNII: 2KR89I4H1Y)
BENZYL ALCOHOL (UNII: LKG8494WBH)
CAPRYLYL GLYCOL (UNII: 00YIU5438U)
DISODIUM STEAROYL GLUTAMATE (UNII: 45ASM2L11M)
MALTODEXTRIN (UNII: 7CVR7L4A2D)
METHYLPARABEN (UNII: A2I8C7HI9T)
PALMITIC ACID (UNII: 2V16EO95H1)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
RETINYL LINOLEATE (UNII: 61911N8D6W)
SODIUM COCOYL GLUTAMATE (UNII: BMT4RCZ3HG)
STEARIC ACID (UNII: 4ELV7Z65AP)
XANTHAN GUM (UNII: TTV12P4NEE)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 49967-092-01	1 in 1 CARTON	07/01/2011	04/04/2014
1		48 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part352	07/01/2011

Labeler - L'Oreal USA Products Inc (002136794)

Establishment
Name	Address	ID/FEI	Business Operations
L'Oreal USA Products Inc		624244349	manufacture(49967-092)