DRS. ACNE SPOT TREATMENT- salicylic acid gel

Drs. ACNE SPOT TREATMENT by

Drug Labeling and Warnings

Drs. ACNE SPOT TREATMENT by is a Otc medication manufactured, distributed, or labeled by OL PHARMA TECH, LLC Drs. PHARMACY, OL PHARMA TECH, LLC Drs PHARMACY. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Salicylic Acid 2% 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

www.drspharmacyusa.com

PACKAGE LABEL

INGREDIENTS AND APPEARANCE

DRS. ACNE SPOT TREATMENT 
salicylic acid gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 80489-357
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ)	SALICYLIC ACID	20 mg  in 1 g

Inactive Ingredients
Ingredient Name	Strength
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)
CARBOMER INTERPOLYMER TYPE A (55000 CPS) (UNII: 59TL3WG5CO)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 80489-357-01	1 in 1 CARTON	04/13/2024
1		20 g in 1 TUBE, WITH APPLICATOR; Type 0: Not a Combination Product
2	NDC: 80489-357-02	1 in 1 CARTON	04/13/2024
2		30 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 Drug	M006	02/01/2022

Labeler - OL PHARMA TECH, LLC Drs. PHARMACY (021170377)

Registrant - OL PHARMA TECH, LLC Drs PHARMACY (021170377)

Establishment
Name	Address	ID/FEI	Business Operations
OL PHARMA TECH, LLC Drs PHARMACY		021170377	manufacture(80489-357)