ILLUMINATING DAILY MOISTURIZER SPF 15- avobenzone, octinoxate, octisalate lotion 
CVS Pharmacy

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

Avobenzone 3%, Octinoxate 7.5%, Octisalate 2%

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.

In case of accidental ingestion, get medical help or contact a Poison Control Center immediately.

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 value of 15 or higher and other sun protection measures including:

Other information

Inactive ingredients

Water (Aqua), C12-15 Alkyl Benzoate, Diethylhexyl 2,6 Naphthalate, Cetearyl Alcohol, Dimethicone, Glycine Soja (Soybean) Seed Extract, Glyceirn, BIS-Phenylpropyl Dimethicone, Arachidyl Alcohol, Phenoxyethanol, Cetearyl Glucoside, Panthenol, Benzyl Alcohol, Ethylene/Acrylic Acid Copolymer, Behenyl Alcohol, Steareth-2, Fragrance (Parfum), Steareth-12, Polyacrylamide, Nylon 10-10, Arachidyl Glucoside, Disodium EDTA, C13-14 Isoparaffin, Ethylhexylglycerin, Laureth-7, Benzalkonium Chloride, Sodium Hydroxide, Iodopropynyl Butylcarbamate, BHT, Titanium Dioxide (CI 77891), Mica.

Label Copy

Image of the label

ILLUMINATING DAILY MOISTURIZER SPF 15 
avobenzone, octinoxate, octisalate lotion
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:59779-601
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
AVOBENZONE (UNII: G63QQF2NOX) (AVOBENZONE - UNII:G63QQF2NOX) AVOBENZONE30 mg  in 1 mL
OCTINOXATE (UNII: 4Y5P7MUD51) (OCTINOXATE - UNII:4Y5P7MUD51) OCTINOXATE75 mg  in 1 mL
OCTISALATE (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W) OCTISALATE20 mg  in 1 mL
Inactive Ingredients
Ingredient NameStrength
WATER (UNII: 059QF0KO0R)  
ALKYL (C12-15) BENZOATE (UNII: A9EJ3J61HQ)  
DIETHYLHEXYL 2,6-NAPHTHALATE (UNII: I0DQJ7YGXM)  
CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)  
DIMETHICONE (UNII: 92RU3N3Y1O)  
SOYBEAN (UNII: L7HT8F1ZOD)  
GLYCERIN (UNII: PDC6A3C0OX)  
BIS-PHENYLPROPYL DIMETHICONE (15 CST) (UNII: 4836494CFT)  
ARACHIDYL ALCOHOL (UNII: 1QR1QRA9BU)  
PHENOXYETHANOL (UNII: HIE492ZZ3T)  
CETEARYL GLUCOSIDE (UNII: 09FUA47KNA)  
PANTHENOL (UNII: WV9CM0O67Z)  
BENZYL ALCOHOL (UNII: LKG8494WBH)  
ACRYLIC ACID/ETHYLENE COPOLYMER (600 MPA.S) (UNII: 1PEZ3NLY6I)  
DOCOSANOL (UNII: 9G1OE216XY)  
STEARETH-2 (UNII: V56DFE46J5)  
STEARETH-21 (UNII: 53J3F32P58)  
POLYACRYLAMIDE (10000 MW) (UNII: E2KR9C9V2I)  
NYLON-12 (UNII: 446U8J075B)  
ARACHIDYL GLUCOSIDE (UNII: 6JVW35JOOJ)  
EDETATE DISODIUM (UNII: 7FLD91C86K)  
C13-14 ISOPARAFFIN (UNII: E4F12ROE70)  
ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)  
LAURETH-7 (UNII: Z95S6G8201)  
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7)  
SODIUM HYDROXIDE (UNII: 55X04QC32I)  
IODOPROPYNYL BUTYLCARBAMATE (UNII: 603P14DHEB)  
BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K)  
TITANIUM DIOXIDE (UNII: 15FIX9V2JP)  
MICA (UNII: V8A1AW0880)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:59779-601-05118 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product04/13/2018
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart35204/13/2018
Labeler - CVS Pharmacy (062312574)
Registrant - Apollo Health and Beauty Care Inc. (201901209)
Establishment
NameAddressID/FEIBusiness Operations
Apollo Health and Beauty Care Inc.201901209manufacture(59779-601)

Revised: 4/2018
Document Id: c5a16bf6-0921-440e-ba11-be811fb21410
Set id: 270383c8-1048-4a5d-a253-20755be2c006
Version: 1
Effective Time: 20180416
 
CVS Pharmacy