GLYTONE HYDRA LIPID UV MINERAL SUNSCREEN SPF 40 PLUS- zinc oxide, titanium dioxide lotion 
Pierre Fabre USA Inc.

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Glytone Hydra Lipid UV Mineral Sunscreen SPF 40 PLUS

Drug Facts

Purpose

Sunscreen

Active ingredients

Titanium Dioxide 2%

Zinc Oxide 1%

Uses

Warnings

For external use only

Do not use on damaged or broken skin

When using this product keep out of eyes. Rinse eyes with water to remove.

Stop use and ask a doctor if rash occurs

Keep out of reach of children. If product is swallowed, get medical help or contact a Poison Control Center right away.

Directions

Sun Protection Measures. Spending time in the sun increases your risk of skin cancer and early skin aging. To decrease this risk, regularly use a sunscreen with a broad spectrum SPF of 15 or higher and other sun protection measures including:

Other information

Inactive ingredients

Water, Butyloctyl Salicylate, Octyldodecyl Neopentanoate, Ethylhexyl Isononanoate, Polyester-7, Glycerin, Neopentyl Glycol, Diheptanoate, Cetyl Alcohol, Glyceryl Stearate, Squalane, Phenoxyethanol, PEG-75 Stearate, Bisabolol, Hydrolyzed Sodium Hyaluronate, Pyrus Malus (Apple) Fruit Extract, C12-15 Alkyl Benzoate, Lysolecithin, Sclerotlum Gum, Dimethiconol/Octylsilsesquioxane/Silicate Crosspolymer, Allantoin, Ceteth-20, Steareth-20, Caprylyl Glycol, Triceteareth-4 Phosphate. Pullulan. Xanthan Gum, Sodium Hyaluronate, Dimethiconol/Propylsilsesquioxane/Silicate Crosspolymer
Disodium EDTA, Ethylhexylglycerin, Hexylene Glycol, Dicrateria Rotunda Oil, Ruttnera Lamellosa Oil, Lecithin, Silica, Camellia Sinensis Leaf Extract, Avena Sativa (Oat) Kernel Extract, Sodium Ascorbate, Potassium Sorbate, Tocopherol.

Questions or comments?

visit www.glytone.com or call toll-free 800-GLYTONE (459-8663)

Indications

Apply generously 15 minutes before sun exposure

etc

Keep out of reach of children.

If swallowed, call a Poison Control Center right away.

Do not use

On broken skin

Principal Display Panel - 50 mL Carton

GLYTONE

Hyda Lipid UV

Mineral Sunscreen

Broad spectrum SPF 40+

Sun Protection

Hyaluronic Acid

Squalane

Titanium Dioxide

Zinc Oxide

FRAGRANCE-FREE

50 mL / 1.7 FL. OZ.

Glytone Mineral Sunscreen

GLYTONE HYDRA LIPID UV MINERAL SUNSCREEN  SPF 40 PLUS
zinc oxide, titanium dioxide lotion
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:64760-720
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (TITANIUM DIOXIDE - UNII:15FIX9V2JP) TITANIUM DIOXIDE2 mg  in 50 mL
ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC OXIDE - UNII:SOI2LOH54Z) ZINC OXIDE1 mg  in 50 mL
Inactive Ingredients
Ingredient NameStrength
OCTYLDODECYL NEOPENTANOATE (UNII: X8725R883T)  
BUTYLOCTYL SALICYLATE (UNII: 2EH13UN8D3)  
PHENOXYETHANOL (UNII: HIE492ZZ3T)  
PEG-75 STEARATE (UNII: OT38R0N74H)  
.BETA.-BISABOLOL (UNII: LP618AV2EA)  
APPLE FRUIT OIL (UNII: 9NT987I3A8)  
HYDROGENATED SOYBEAN LECITHIN (UNII: H1109Z9J4N)  
CAMELLIA SINENSIS FLOWER (UNII: 9I2BJY2J17)  
OAT KERNEL OIL (UNII: 3UVP41R77R)  
SODIUM ASCORBATE (UNII: S033EH8359)  
POTASSIUM SORBATE (UNII: 1VPU26JZZ4)  
ALPHA-TOCOPHEROL, L- (UNII: 82190DH9F2)  
WATER (UNII: 059QF0KO0R)  
ETHYLHEXYL ISONONANOATE (UNII: I6KB4GE3K4)  
GLYCERIN (UNII: PDC6A3C0OX)  
CETYL ALCOHOL (UNII: 936JST6JCN)  
NEOPENTYL GLYCOL DIHEPTANOATE (UNII: 5LKW3C543X)  
DICRATERIA ROTUNDA OIL (UNII: Z0DWU9R4GM)  
SODIUM ACETYLATED HYALURONATE (UNII: WN66R7GL93)  
DIMETHICONOL/PROPYLSILSESQUIOXANE/SILICATE CROSSPOLYMER (450000000 MW) (UNII: 9KB5R958PB)  
DITETRACYCLINE TETRASODIUM EDETATE (UNII: WX0A0IT7K5)  
TRILAURETH-4 PHOSPHATE (UNII: M96W2OLL2V)  
POLYESTER-7 (UNII: 0841698D2F)  
C12-15 ALKYL ETHYLHEXANOATE (UNII: GQJ580CH83)  
LOCUST BEAN GUM (UNII: V4716MY704)  
GLYCERYL STEARATE SE (UNII: FCZ5MH785I)  
SQUALANE (UNII: GW89575KF9)  
ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)  
HEXYLENE GLYCOL (UNII: KEH0A3F75J)  
HYDRATED SILICA (UNII: Y6O7T4G8P9)  
RUTTNERA LAMELLOSA OIL (UNII: 5XZ38R4SUT)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:64760-720-011 in 1 CARTON07/02/202003/31/2026
150 mL in 1 TUBE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM02007/02/202003/31/2026
Labeler - Pierre Fabre USA Inc. (117196928)
Registrant - Pierre Fabre USA Inc. (117196928)

Revised: 4/2024
Document Id: 174052ca-412d-8920-e063-6294a90a6af6
Set id: 9ffa08ea-c450-80b7-e053-2a95a90a4bd6
Version: 5
Effective Time: 20240429
 
Pierre Fabre USA Inc.