WOLF DAILY MOISTURIZIER SPF 15- octinoxate, oxybenzone, zinc oxide lotion 
Apollo Health and Beauty Care Inc.

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

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Drug Facts

Active ingredients

Octinoxate 2%, Oxybenzone 4%, Zince Oxide 3.8%

Purpose

Sunscreen

Use(s)

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.

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 Broad Spectrum SPF value of 15 or higher and other sun protection measure including:

Other information

Protect this product from excessive heat and direct sun.

Inactive ingredients

Water (Aqua), Butylene Glycol Cocoate, Neopentyl Glycol Diheptanoate, Styrene/Acrylates Copolymer, Cetearyl Alcohol, Glycerin, Acetamidoethoxyethanol, Potassium Cetyl Phosphate, Acrylamide/Sodium Acryloyldimethyltaurate Copolymer, Polysorbate 80, Isohexadecane, Benzyl Alcohol, Xanthan Gum, Tetrasodium Glutamate Diacetate, Fragrance (Parfum), Lactic Acid, Triethoxycaprylylsilane, Tetrahexydecyl Ascorbate, Crambe Abyssinica Seed Oil, Panthenol, Hydrolyzed Keratin, Camellia Sinensis Leaf Extract, Aspalathus Linearis Leaf Extract, Aloe Barbadensis Leaf Juice, Pinus Pinaster Bark Extract, Hydrolyzed Adansonia Digitata Seed Extract, Melaleuca Alternifolia (Tea Tree) Leaf Extract, Hydrolyzed Hemp Protein, Hydrolyzed Vegetable Protein, Ascorbyl Glucoside, Phytonadione, Niacinamide, Cyanocobalamin, Tocopheryl Acetate, Iodopropynyl Butylcarbamate.

Questions?

Call toll-free 1-855-760-3569

Label Copy

Image of the label

WOLF DAILY MOISTURIZIER SPF 15 
octinoxate, oxybenzone, zinc oxide lotion
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:63148-008
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
OCTINOXATE (UNII: 4Y5P7MUD51) (OCTINOXATE - UNII:4Y5P7MUD51) OCTINOXATE20 mg  in 1 mL
OXYBENZONE (UNII: 95OOS7VE0Y) (OXYBENZONE - UNII:95OOS7VE0Y) OXYBENZONE40 mg  in 1 mL
ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC CATION - UNII:13S1S8SF37) ZINC CATION38 mg  in 1 mL
Inactive Ingredients
Ingredient NameStrength
WATER (UNII: 059QF0KO0R)  
NEOPENTYL GLYCOL DIHEPTANOATE (UNII: 5LKW3C543X)  
STYRENE/ACRYLAMIDE COPOLYMER (500000 MW) (UNII: 5Z4DPO246A)  
CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)  
GLYCERIN (UNII: PDC6A3C0OX)  
POTASSIUM CETYL PHOSPHATE (UNII: 03KCY6P7UT)  
SODIUM ACRYLOYLDIMETHYLTAURATE-ACRYLAMIDE COPOLYMER (1:1; 90000-150000 MPA.S) (UNII: 5F4963KLHS)  
POLYSORBATE 80 (UNII: 6OZP39ZG8H)  
ISOHEXADECANE (UNII: 918X1OUF1E)  
BENZYL ALCOHOL (UNII: LKG8494WBH)  
XANTHAN GUM (UNII: TTV12P4NEE)  
TETRASODIUM GLUTAMATE DIACETATE (UNII: 5EHL50I4MY)  
LACTIC ACID (UNII: 33X04XA5AT)  
TETRAHEXYLDECYL ASCORBATE (UNII: 9LBV3F07AZ)  
CRAMBE HISPANICA SUBSP. ABYSSINICA SEED OIL (UNII: 0QW9S92J3K)  
IODOPROPYNYL BUTYLCARBAMATE (UNII: 603P14DHEB)  
PANTHENOL (UNII: WV9CM0O67Z)  
GREEN TEA LEAF (UNII: W2ZU1RY8B0)  
ASPALATHUS LINEARIS LEAF (UNII: H7UGK1GJCU)  
ALOE VERA LEAF (UNII: ZY81Z83H0X)  
MARITIME PINE (UNII: 50JZ5Z98QY)  
ADANSONIA DIGITATA SEED (UNII: 2936P60TPX)  
TEA TREE OIL (UNII: VIF565UC2G)  
CANNABIS SATIVA SEED (UNII: QE567Z26NG)  
ASCORBYL GLUCOSIDE (UNII: 2V52R0NHXW)  
PHYTONADIONE (UNII: A034SE7857)  
NIACINAMIDE (UNII: 25X51I8RD4)  
CYANOCOBALAMIN (UNII: P6YC3EG204)  
.ALPHA.-TOCOPHEROL ACETATE, DL- (UNII: WR1WPI7EW8)  
TRIETHOXYCAPRYLYLSILANE (UNII: LDC331P08E)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:63148-008-04118 mL in 1 TUBE; Type 0: Not a Combination Product06/01/2018
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart35206/01/2018
Labeler - Apollo Health and Beauty Care Inc. (201901209)
Registrant - Apollo Health and Beauty Care Inc. (201901209)
Establishment
NameAddressID/FEIBusiness Operations
Apollo Health and Beauty Care Inc.201901209manufacture(63148-008)

Revised: 6/2018
Document Id: c906efd9-39f7-4ce5-bbf2-2a280d095438
Set id: 6f806d1d-c5f0-4a87-87f7-aa81033ae3b1
Version: 1
Effective Time: 20180601
 
Apollo Health and Beauty Care Inc.