OLP ACNE CLEAR- salicylic acid gel 
OHIO LAB PHARMA

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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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

  • store at 15-30 C ( 59-86 F)
  • close cap tightly after use
  • keep away from heat

QUESTIONS

ohiolabpharma.us

PACKAGE LABEL

acne gel

OLP ACNE CLEAR 
salicylic acid gel
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:70648-300
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:70648-300-011 in 1 CARTON02/01/2017
120 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 finalpart333D02/01/201708/01/2017
Labeler - OHIO LAB PHARMA (080215854)
Registrant - OHIO LAB PHARMA (080215854)
Establishment
NameAddressID/FEIBusiness Operations
OHIO LAB PHARMA080215854manufacture(70648-300)

Revised: 8/2020
 
OHIO LAB PHARMA