SPOT ACNE TREATMENT- salicylic acid gel 
Walgreens

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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Well at Walgreens

Drug Facts

Active ingredients                 Purpose

Salicylic Acid - 2.0%              Acne Medication 

Use

Helps prevent new acne blemishes

For external use only
Flammable, keep away from oipen fire or flame

When using this product skin irritation and dryness is more likely 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 the children
If product is swallowed, get medical help or contact a Poison Control Center right away

Avoid contact with eyes. If contact occurs, flush thoroughly with water

Directions

Cleanse thoroughly before applying treatment
Cover the entire affected area with a thin layer one to three times daily.
Because of excessive drying of the skin may occurs, 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 usage to once a day or every other day.

Inactive ingredients

Alcohol
Ammonium Hydroxide
Benzalkonium Chloride
Butylene Glycol
C12-15 Alkyl Lactate
C13-14 Isoparaffin
Capryloyl Glycine
Cedrus Atlantica Bark Extract
Cetyl Lactate
Cinnamomum Zeylanicum Bark Extract
Cocamidopropyl PG-Dimonium Chloride Phosphate
Cyclopentasiloxane
Dehydroxanthan Gum
Denatonium Benzoate
Fragrance
Glycerin
Hamamelis Virginiana (Witch Hazel) Water
Laureth-7
Phenoxyethanol
Polyacrylamide
Polysorbate 20
Portulaca Oleracea Extract
PPG-2 Isoceteth-20 Acetate
Propylene Glycol
Sarcosine
t-Butyl Alcohol
Tetrasodium EDTA
Water

image descriptionimage description

SPOT ACNE TREATMENT 
salicylic acid gel
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:0363-7782
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
Salicylic Acid (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ) Salicylic Acid2 g  in 100 g
Inactive Ingredients
Ingredient NameStrength
Alcohol (UNII: 3K9958V90M)  
AMMONIA (UNII: 5138Q19F1X)  
Benzalkonium Chloride (UNII: F5UM2KM3W7)  
Butylene Glycol (UNII: 3XUS85K0RA)  
C12-15 Alkyl Lactate (UNII: GC844VRD7E)  
C13-14 Isoparaffin (UNII: E4F12ROE70)  
Capryloyl Glycine (UNII: 8TY5YO42NJ)  
CEDRUS ATLANTICA BARK (UNII: ITP1Q41UPF)  
Cetyl Lactate (UNII: A7EVH2RK4O)  
CINNAMON BARK OIL (UNII: XE54U569EC)  
Cocamidopropyl PG-Dimonium Chloride Phosphate (UNII: H2KVQ74JM4)  
CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)  
Dehydroxanthan Gum (UNII: 63ZP7I1BQO)  
Denatonium Benzoate (UNII: 4YK5Z54AT2)  
Glycerin (UNII: PDC6A3C0OX)  
HAMAMELIS VIRGINIANA TOP WATER (UNII: NT00Y05A2V)  
Laureth-7 (UNII: Z95S6G8201)  
Phenoxyethanol (UNII: HIE492ZZ3T)  
Polysorbate 20 (UNII: 7T1F30V5YH)  
PURSLANE (UNII: M6S840WXG5)  
PPG-2 Isoceteth-20 Acetate (UNII: BI6C7YO419)  
Propylene Glycol (UNII: 6DC9Q167V3)  
Sarcosine (UNII: Z711V88R5F)  
TERT-BUTYL ALCOHOL (UNII: MD83SFE959)  
EDETATE SODIUM (UNII: MP1J8420LU)  
WATER (UNII: 059QF0KO0R)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:0363-7782-0121 g in 1 TUBE; Type 0: Not a Combination Product04/17/2018
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart333D04/17/2018
Labeler - Walgreens (008965063)
Registrant - Product Quest Mfg (927768135)
Establishment
NameAddressID/FEIBusiness Operations
Product Quest Mfg927768135manufacture(0363-7782)

Revised: 4/2018
Document Id: 7f7e19da-a5d0-407c-a6b5-030248746e63
Set id: bebe2d42-09af-4ed3-b74a-394830bc32e4
Version: 1
Effective Time: 20180430
 
Walgreens