Oxy daily defense exfoliating face scrub gel

Active ingredient

Salicylic acid 2%


Acne treatment


treats and helps prevent acne


For external use only

When using this product

  • keep away from eyes. If contact occurs, flush thoroughly with water.
  • skin irritation and dryness is more likely to occur if you use another topical acne medication at the same time. If irritation occurs, only use one topical acne medication at a time.

If pregnant or breast-feeding

ask a health professional before use.

Keep out of reach of children

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


  • wet face
  • squeeze scrub into hands and massage gently over face and neck
  • rinse thoroughly and pat dry
  • because too much drying of the skin may occur, start with 1 use, then gradually increase to 2 or 3 times daily if needed or as directed by a doctor
  • if bothersome dryness or peeling occurs, reduce usage to once a day or every other day

Inactive ingredients

acrylates copolymer, aloe barbadensis leaf juice, aluminum powder, anhydrous citric acid, astragalus membranaceus root extract, butyl methoxydibenzoylmethane, caprylyl glycol, cocamidopropyl betaine, D&C violet no. 2, edetate disodium, ethylhexyl palmitate, ethylhexyl salicylate, ethylhexyl methoxycinnamate, FD&C blue no. 1, forsythia suspensa fruit extract, fragrance, glycerin, PEG-40 hydrogenated castor oil, PEG-8/SMDI copolymer, petrolatum, phenoxyethanol, polyethylene, potassium C12-13 alkyl phosphate, potassium sorbate, PPG-26-buteth-26, purified water, silica, sodium benzoate, sodium C14-16 olefin sulfonate, sorbic acid, trolamine


1-877-636-2677MON-FRI 9 AM-5 PM (EST)

Ingredients and appearance - Product information

Oxy daily defense exfoliating face scrub gel- Salicylic acid

Product information

Product Type HUMAN OTC DRUG LABEL Item Code (Source) NDC: 10742-8306
Route of Administration Topical

Active Ingredient/Active Moiety

Ingredient Name Strength
Salicylic acid ( UNII: O414PZ4LPZ)( Salicylic acid - UNII: O414PZ4LPZ ) 20 mgin 1 g

Inactive Ingredients

Ingredient Name Code
Carbomer copolymer type b (allyl pentaerythritol crosslinked) ( UNII: 809Y72KV36)
Aloe vera leaf ( UNII: ZY81Z83H0X)
Aluminum ( UNII: CPD4NFA903)
Anhydrous citric acid ( UNII: XF417D3PSL)
Astragalus propinquus root ( UNII: 922OP8YUPF)
Avobenzone ( UNII: G63QQF2NOX)
Caprylyl glycol ( UNII: 00YIU5438U)
Cocamidopropyl betaine ( UNII: 5OCF3O11KX)
D&c violet no. 2 ( UNII: 350KA7O6HK)
Edetate disodium ( UNII: 7FLD91C86K)
Ethylhexyl palmitate ( UNII: 2865993309)
Octisalate ( UNII: 4X49Y0596W)
Octinoxate ( UNII: 4Y5P7MUD51)
Fd&c blue no. 1 ( UNII: H3R47K3TBD)
Forsythia suspensa fruit ( UNII: P4793M1ES5)
Glycerin ( UNII: PDC6A3C0OX)
Polyoxyl 40 hydrogenated castor oil ( UNII: 7YC686GQ8F)
Peg-8/smdi copolymer ( UNII: CCX72L6NY6)
Petrolatum ( UNII: 4T6H12BN9U)
Phenoxyethanol ( UNII: HIE492ZZ3T)
Potassium sorbate ( UNII: 1VPU26JZZ4)
Ppg-26-buteth-26 ( UNII: 2II1K6TZ4P)
Water ( UNII: 059QF0KO0R)
Silicon dioxide ( UNII: ETJ7Z6XBU4)
Sodium benzoate ( UNII: OJ245FE5EU)
Sodium c14-16 olefin sulfonate ( UNII: O9W3D3YF5U)
Sorbic acid ( UNII: X045WJ989B)
Trolamine ( UNII: 9O3K93S3TK)

Product Characteristics

Marketing Information

Marketing Category Application Number or Monograph Citation Territorial Authority Marketing Start Date
OTC monograph final part333D USA

Labeler - The Mentholatum Company( 002105757)

Package/label principal display panel