ACNE CORRECTION PADS- salicylic acid cloth

Acne Correction Pads by

Drug Labeling and Warnings

Acne Correction Pads by is a Otc medication manufactured, distributed, or labeled by Private Label Skin Care. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Drug Facts

Active ingredient

Salicylic Acid 2%

Purpose

Acne Treatment

Uses

for the treatment of acne

Warnings

For external use only

Do not use on broken skin or large areas of the skin

When using this product skin irritation and dryness is more likely to occur if you use another topical acne medication at the same time. If irritation occurs, only use one topical acne medication at a time. avoid contact with eyes, lips and mouth. If contact occurs, flush thoroughly with water.

Keep out of reach of children If swallowed, get medical help or contact a Poison Control Center right away.

Directions 

Apply evenly over face and neck avoiding eye area. Allow to absorb before applying additional products. Can be used twice daily or as directed by physician. Do not rinse. Tighten cap after use to prevent pads from drying out.

Inactive ingredients 

Water/Aqua/Eau, Lactic Acid, Glycolic Acid, Ethoxydiglycol, Sodium Hydroxide, Glycerin, Cucumber (Cucumis Sativus) Fruit Extract, Orange (Citrus Aurantium Dulcis) Peel Extract, Aloe Vera (Aloe Barbadensis) Leaf Extract, Matricaria (Chamomilla Recutita) Flower Extract, Grapefruit (Citrus Grandis) Peel Extract, PEG-40 Hydrogenated Castor Oil, PPG-26-Buteth-26, Dipotassium Glycyrrhizate, Caprylic/Capric Triglyceride, Menthyl Lactate, Allantoin, Tetrasodium EDTA, Beta-Glucan, Methylchloroisothiazolinone, Methylisothiazolinone

SPL UNCLASSIFIED SECTION

brand MD

Glycolic Acid 5% + Lactic Acid 5% + Aloe

MEDICAL GRADE

CLEAR

RECOMMENDED FOR
BLEMISH-PRONE
COMBO    NORMAL
DRY          OILY

GREEN LEAF PROGRAM

NOT TESTED ON ANIMALS

Distributed by:
brandMD®
Canoga Park, CA 91304
(818) 534-3180
www.brandMD.com

Packaging

INGREDIENTS AND APPEARANCE

ACNE CORRECTION PADS 
salicylic acid cloth

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 72957-012(NDC:39765-029)
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ)	SALICYLIC ACID	2 g  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
LACTIC ACID, UNSPECIFIED FORM (UNII: 33X04XA5AT)
GLYCOLIC ACID (UNII: 0WT12SX38S)
DIETHYLENE GLYCOL MONOETHYL ETHER (UNII: A1A1I8X02B)
SODIUM HYDROXIDE (UNII: 55X04QC32I)
GLYCERIN (UNII: PDC6A3C0OX)
CUCUMBER (UNII: YY7C30VXJT)
ORANGE PEEL (UNII: TI9T76XD44)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
CHAMOMILE (UNII: FGL3685T2X)
CITRUS MAXIMA FRUIT RIND (UNII: 5NX3G75CA6)
POLYOXYL 40 HYDROGENATED CASTOR OIL (UNII: 7YC686GQ8F)
PPG-26-BUTETH-26 (UNII: 2II1K6TZ4P)
GLYCYRRHIZINATE DIPOTASSIUM (UNII: CA2Y0FE3FX)
MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U)
MENTHYL LACTATE, (-)- (UNII: 2BF9E65L7I)
ALLANTOIN (UNII: 344S277G0Z)
EDETATE SODIUM (UNII: MP1J8420LU)
1,3-BETA-GLUCAN SYNTHASE COMPONENT FKS1 (UNII: 4FRY3LJG0V)
METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN)
METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 72957-012-01	60 in 1 JAR	01/01/2025
1		1.2 mL in 1 PACKAGE; 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	01/01/2025

Labeler - Private Label Skin Care (116996962)

Establishment
Name	Address	ID/FEI	Business Operations
Private Label Skin Care		116996962	relabel(72957-012)