OLP ACNE CLEAR- salicylic acid gel

OLP ACNE CLEAR by

Drug Labeling and Warnings

OLP ACNE CLEAR by is a Otc medication manufactured, distributed, or labeled by OHIO LAB PHARMA. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

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

INACTIVE INGREDIENT

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

OLP ACNE GEL

INGREDIENTS AND APPEARANCE

OLP ACNE CLEAR 
salicylic acid gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 70648-300
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ)	SALICYLIC ACID	5 mg  in 1 g

Inactive Ingredients
Ingredient Name	Strength
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 Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 70648-300-01	1 in 1 CARTON	02/01/2017
1		20 g in 1 TUBE, WITH APPLICATOR; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph final	part333D	02/01/2017

Labeler - OHIO LAB PHARMA (080215854)

Registrant - OHIO LAB PHARMA (080215854)

Establishment
Name	Address	ID/FEI	Business Operations
OHIO LAB PHARMA		080215854	manufacture(70648-300)