BLUE HERBAL SPOT TREATMENT SALICYLIC ACID ACNE TREATMENT- salicylic acid gel 
L'Oreal USA Products Inc

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Drug Facts

Active ingredient

Salicylic Acid 2%

Purpose

Acne treatment

Use

  • for the treatment of acne

Warnings

For external use only

When using this products

  • 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.

Keep out of reach of children.

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

Directions

  • clean the skin thoroughly before applying this product
  • cover the entire affected area with a thin layer one to three times daily
  • because excessive drying of the skin may occur, start with one application daily, then gradually increase to two or three times daily if needed or as directed by a doctor
  • if bothersome dryness or peeling occurs, reduce application to once a day or every other day

Inactive ingredients

water, alcohol denat., glycerin, butylene glycol, methyl methacrylate crosspolymer, ammonium polyacryloyldimethyl taurate, perlite, nylon-12, dipropylene glycol, xanthan gum, peumus boldus leaf extract, boswellia serrata extract, hamamelis virginiana (witch hazel) water, t-butyl alcohol, camphor, menthol, zingiber officinale (ginger) root extract, sanuisorba officinalis root extract, cinnamomum cassia bark extract, phenoxyethanol, cinnamal, laminaria saccharina extract, zinc sulfate, pyridoxine HCl, sodium hydroxide, citric acid

Questions or comments?

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BLUE HERBAL SPOT TREATMENT SALICYLIC ACID ACNE TREATMENT 
salicylic acid gel
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:49967-602
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ) SALICYLIC ACID20 mg  in 1 mL
Inactive Ingredients
Ingredient NameStrength
WATER (UNII: 059QF0KO0R)  
ALCOHOL (UNII: 3K9958V90M)  
GLYCERIN (UNII: PDC6A3C0OX)  
BUTYLENE GLYCOL (UNII: 3XUS85K0RA)  
METHYL METHACRYLATE/GLYCOL DIMETHACRYLATE CROSSPOLYMER (UNII: EG97988M5Q)  
PERLITE (UNII: 0SG101ZGK9)  
NYLON-12 (UNII: 446U8J075B)  
DIPROPYLENE GLYCOL (UNII: E107L85C40)  
XANTHAN GUM (UNII: TTV12P4NEE)  
PEUMUS BOLDUS LEAF (UNII: Q4EWM09M3O)  
INDIAN FRANKINCENSE (UNII: 4PW41QCO2M)  
HAMAMELIS VIRGINIANA LEAF WATER (UNII: 8FP93ED6H2)  
TERT-BUTYL ALCOHOL (UNII: MD83SFE959)  
CAMPHOR (SYNTHETIC) (UNII: 5TJD82A1ET)  
MENTHOL, UNSPECIFIED FORM (UNII: L7T10EIP3A)  
GINGER (UNII: C5529G5JPQ)  
SANGUISORBA OFFICINALIS ROOT (UNII: 4NYV2HT01X)  
CHINESE CINNAMON (UNII: WS4CQ062KM)  
PHENOXYETHANOL (UNII: HIE492ZZ3T)  
SACCHARINA LATISSIMA (UNII: 68CMP2MB55)  
ZINC SULFATE (UNII: 89DS0H96TB)  
PYRIDOXINE HYDROCHLORIDE (UNII: 68Y4CF58BV)  
SODIUM HYDROXIDE (UNII: 55X04QC32I)  
CITRIC ACID ACETATE (UNII: DSO12WL7AU)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:49967-602-011 in 1 CARTON01/01/201601/01/2016
115 mL in 1 TUBE; Type 0: Not a Combination Product
2NDC:49967-602-021.5 mL in 1 PACKET; Type 0: Not a Combination Product01/01/201601/01/2016
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM00601/01/201601/01/2016
Labeler - L'Oreal USA Products Inc (002136794)
Establishment
NameAddressID/FEIBusiness Operations
Cosmetic Essence, LLC032565959manufacture(49967-602)
Establishment
NameAddressID/FEIBusiness Operations
Paklab177711082pack(49967-602)
Establishment
NameAddressID/FEIBusiness Operations
L'OREAL USA, INC.185931458analysis(49967-602)

Revised: 1/2024
 
L'Oreal USA Products Inc