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Dollar General Acne Spot Medication

Medically reviewed by Drugs.com. Last updated on Jun 30, 2021.

Dosage form: gel
Ingredients: SALICYLIC ACID 20mg in 1mL
Labeler: DOLGENCORP, LLC
NDC Code: 55910-601

DRUG FACTS

Active ingredient                                 Purpose

Salicylic Acid 2%............................................Acne medication



Uses
for the treatment of acne


Keep out of reach of children. If swallowed, get medical help or contact a
Poison Control Center right away. Avoid contact with eyes. If contact occurs,
flush thoroughly with water.



Uses for the treatment of acne

Warnings

For external use only


Flammable, keep away from open fire or flame


When using this product
and other topical acne medications at the same time
or immediately following use of this product, increased dryness or irritation of the skin
may occur. If this occurs, only one medication  should be used unless directed by a doctor.


Keep out of reach of children. If 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 skin thoroughly before applying medication
- Cover the affected area entirely up to three times daily
- If excessive dryness or peeling occurs, reduce usage to once a day or every other day
- Recommended for daily use

Inactive Ingredients


Alcohol, Butylene Glycol, Capryloyl Glycine, Cedrus Atlantic Bark Extract, Cinnamomum
Zeylanicum Bark Extract, Hexylene Glycol, Hydroxyethylcellulose, Methylparaben,
Portulica Oleracea Extract, PPG-2 Isoceth-20 Acetate, Propylene Glycol, Propylparaben,
Sarcosine, Sodium Citrate, Water



DOLLAR GENERAL ACNE SPOT MEDICATION 
salicylic acid gel
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:55910-601
Route of AdministrationTOPICALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
SALICYLIC ACID (SALICYLIC ACID) SALICYLIC ACID20 mg  in 1 mL
Inactive Ingredients
Ingredient NameStrength
WATER 
BUTYLENE GLYCOL 
MANGANESE GLUCONATE 
OLIVE OIL 
CEDRUS ATLANTICA BARK 
GLYCERIN 
HEXYLENE GLYCOL 
PURSLANE 
ANHYDROUS TRISODIUM CITRATE 
ALCOHOL 
METHYLPARABEN 
PROPYLPARABEN 
HYDROXYETHYL CELLULOSE (4000 MPA.S FOR 1% AQUEOUS SOLUTION) 
Packaging
#Item CodePackage Description
1NDC:55910-601-561 TUBE (TUBE) in 1 CARTON
122 mL in 1 TUBE
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333D07/10/2010
Labeler - DOLGENCORP, LLC (068331990)
Registrant - Pharma Pac, LLC (140807475)
Establishment
NameAddressID/FEIOperations
Pharma Pac, LLC140807475manufacture

 
DOLGENCORP, LLC

Further information

Always consult your healthcare provider to ensure the information displayed on this page applies to your personal circumstances.