EQUATE SPF 70 ULTRA SUNSCREEN- avobenzone, homosalate, octisalate, octocrylene, oxybenzone lotion 
Wal-Mart Stores 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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Walmart Equate SPF 70 Ultra Sunscreen Lotion

Active ingredients

Avobenzone 3.0%, Homosalate 15.0%, Octisalate 5.0%, Octocrylene 10.0%, Oxybenzone 6.0%

Purpose

Sunscreen

Uses

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

Other information

Inactive ingredients

water, butylene glycol, microcrystalline cellulose, glyceryl stearate, behenyl alcohol, butylated PVP, benzyl alcohol, palmitic acid, myristyl alcohol, caprylic/capric triglyceride, stearic acid, lauryl alcohol, cetyl alcohol, sodium ascorbyl phosphate, tocopherol (vitamin E), lecithin, cellulose gum, chlorphenesin, disodium EDTA, fragrance.

Label

EQ08160A3

EQUATE  SPF 70 ULTRA SUNSCREEN
avobenzone, homosalate, octisalate, octocrylene, oxybenzone lotion
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:49035-760
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
OXYBENZONE (UNII: 95OOS7VE0Y) (OXYBENZONE - UNII:95OOS7VE0Y) OXYBENZONE60 mg  in 1 mL
HOMOSALATE (UNII: V06SV4M95S) (HOMOSALATE - UNII:V06SV4M95S) HOMOSALATE150 mg  in 1 mL
OCTISALATE (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W) OCTISALATE50 mg  in 1 mL
OCTOCRYLENE (UNII: 5A68WGF6WM) (OCTOCRYLENE - UNII:5A68WGF6WM) OCTOCRYLENE100 mg  in 1 mL
AVOBENZONE (UNII: G63QQF2NOX) (AVOBENZONE - UNII:G63QQF2NOX) AVOBENZONE30 mg  in 1 mL
Inactive Ingredients
Ingredient NameStrength
WATER (UNII: 059QF0KO0R)  
GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)  
MICROCRYSTALLINE CELLULOSE (UNII: OP1R32D61U)  
MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U)  
PALMITIC ACID (UNII: 2V16EO95H1)  
CETYL ALCOHOL (UNII: 936JST6JCN)  
CHLORPHENESIN (UNII: I670DAL4SZ)  
N-VINYLPYRROLIDINONE (UNII: 76H9G81541)  
BUTYLENE GLYCOL (UNII: 3XUS85K0RA)  
DOCOSANOL (UNII: 9G1OE216XY)  
STEARIC ACID (UNII: 4ELV7Z65AP)  
LAURYL ALCOHOL (UNII: 178A96NLP2)  
MYRISTYL ALCOHOL (UNII: V42034O9PU)  
CARBOXYMETHYLCELLULOSE SODIUM, UNSPECIFIED FORM (UNII: K679OBS311)  
LECITHIN, SOYBEAN (UNII: 1DI56QDM62)  
TOCOPHEROL (UNII: R0ZB2556P8)  
BENZYL ALCOHOL (UNII: LKG8494WBH)  
EDETATE DISODIUM ANHYDROUS (UNII: 8NLQ36F6MM)  
SODIUM ASCORBYL PHOSPHATE (UNII: 836SJG51DR)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:49035-760-12236 mL in 1 TUBE; Type 0: Not a Combination Product06/04/2019
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart35206/04/2019
Labeler - Wal-Mart Stores Inc (051957769)

Revised: 10/2022
Document Id: ec25f956-0368-b449-e053-2995a90a657a
Set id: 8f24e301-3fce-f9e3-e053-2a95a90affe4
Version: 2
Effective Time: 20221029
 
Wal-Mart Stores Inc