DRS. ACNE CLEAR- salicylic acid gel 
OL PHARMA TECH, LLC Drs. PHARMACY

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ACTIVE INGREDIENT

Salicylic Acid 0.5% w/w.

PURPOSE

Acne treatment

USES

For the treatment of acne. Dries and clears acne pimples, blackheads and whiteheads and allows skin to heal.

DO NOT USE

if you have sensitive skin or are sensitive to salicylic acid

DIRECTIONS

Morning and evening, after a thorough cleansing of the skin, apply acne clear gel locally on cutanous imperfections. Then apply the usual day or night cream. Renew application 1 to 3 times daily.

WARNINGS

For external use only. Using other topical acne medications at the same time or immediately following use of this product may increase dryness or irritation of the skin. If this occurs, only one medication should be used unless directed by a doctor. Avoid direct contact with the eyes. If product gets into the eyes, rinse liberally with water. Discontinue use if skin irritation develops or increases. If irritation persists, consult a doctor.

WHEN USING THIS PRODUCT

Avoid contact with eyes, lips, and mouth.

KEEP OUT OF REACH OF CHILDREN

if swallowed, get medical help or contact poison control center right away

carbomer interpolymer type A, trolamine, vitamin E, propylene glycol, water, isopropyl alcohol, methyl paraben, EDTA, propyl paraben, DMDM hydantoin

OTHER INFORMATION

QUESTIONS

www.drspharmacyusa.com

PACKAGE LABEL

acne clear

DRS. ACNE CLEAR 
salicylic acid gel
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:80489-300
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ) SALICYLIC ACID5 mg  in 1 g
Inactive Ingredients
Ingredient NameStrength
CARBOMER INTERPOLYMER TYPE A (55000 CPS) (UNII: 59TL3WG5CO)  
WATER (UNII: 059QF0KO0R)  
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
.ALPHA.-TOCOPHEROL (UNII: H4N855PNZ1)  
METHYLPARABEN (UNII: A2I8C7HI9T)  
EDETATE DISODIUM (UNII: 7FLD91C86K)  
TROLAMINE (UNII: 9O3K93S3TK)  
ISOPROPYL ALCOHOL (UNII: ND2M416302)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:80489-300-011 in 1 CARTON02/01/2022
120 g in 1 TUBE, WITH APPLICATOR; Type 0: Not a Combination Product
2NDC:80489-300-021 in 1 CARTON02/01/2022
230 g in 1 TUBE, WITH APPLICATOR; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM00602/01/2022
Labeler - OL PHARMA TECH, LLC Drs. PHARMACY (021170377)
Registrant - OL PHARMA TECH, LLC Drs PHARMACY (021170377)
Establishment
NameAddressID/FEIBusiness Operations
OL PHARMA TECH, LLC Drs PHARMACY021170377manufacture(80489-300)

Revised: 10/2023
Document Id: 073aae7e-403b-90f0-e063-6294a90a9ba6
Set id: d6faa57c-d081-b57c-e053-2a95a90a7926
Version: 11
Effective Time: 20231008
 
OL PHARMA TECH, LLC Drs. PHARMACY