TULA SKINCARE KEEP IT CLEAR ACNE FOAM CLEANSER- salicylic acid liquid

Tula Skincare Keep It Clear Acne Foam Cleanser by

Drug Labeling and Warnings

Tula Skincare Keep It Clear Acne Foam Cleanser by is a Otc medication manufactured, distributed, or labeled by The Procter & Gamble Manufacturing Company. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Salicylic Acid 2.0%

PURPOSE

Acne Treatment

Uses

For the treatment of acne. Helps prevent the development of new blemishes.

WARNINGS

For external use only

When using this product

• Avoid contact with the eyes. If contact occurs, rinse thoroughly with water.
• 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.
• If irritation occurs, rinse thoroughly with water.

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

Direction

Clean the skin thoroughly before applying this product.

Massage the entire affected area with one to two pumps & rinse with warm water. Use dailiy, AM & PM

Because excessive drying of the skin may occur, start with one application daily, then increase to two times daily if needed or as directed by a doctor.
If bothersome dryness or peeling occurs, reduce application to once a day or every other day.

INACTIVE INGREDIENT

Aqua/Water/Eau, Sodium Methyl 2-Sulfolaurate, Disodium 2-Sulfolaurate, Disodium Laureth Sulfosuccinate, Lactococcus Ferment Lysate, Melaleuca Alternifolia (Tea Tree) Leaf Oil, Azelaic Acid, Morinda Citrifolia Extract, Glycyrrhiza Glabra (Licorice) Root Extract, Vaccinium Angustifolium (Blueberry) Fruit Extract, Zingiber Officinale (Ginger) Root Extract, Lactic Acid, Hydrolyzed Algin, Glycerin, Citric Acid, Phospholipids, Caprylyl Glycol, Sodium Chloride, Benzoic Acid, Sodium Hydroxide, Sodium Glycolate, Trisodium Dicarboxymethyl Alaninate, Butylene Glycol, Chlorphenesin, Sodium Benzoate, Ethylhexylglycerin, Phenoxyethanol

QUESTIONS

Questions or Comments?

1-844-545-1236

SPL UNCLASSIFIED SECTION

DIST BY TULA LIFE, INC. NY, NY 10065

PRINCIPAL DISPLAY PANEL

TULA

SKINCARE

keep it clear

acne foam

cleanser

salicyclic acid acne treatment

6.3 FL OZ/180 mL

INGREDIENTS AND APPEARANCE

TULA SKINCARE KEEP IT CLEAR ACNE FOAM CLEANSER 
salicylic acid liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 84126-237
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
CAPRYLYL GLYCOL (UNII: 00YIU5438U)
SODIUM HYDROXIDE (UNII: 55X04QC32I)
GLYCERIN (UNII: PDC6A3C0OX)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
DISODIUM LAURETH SULFOSUCCINATE (UNII: D6DH1DTN7E)
MORINDA CITRIFOLIA FRUIT (UNII: 7829X3G2X5)
BENZOIC ACID (UNII: 8SKN0B0MIM)
LACTIC ACID (UNII: 33X04XA5AT)
ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
SODIUM METHYL 2-SULFOLAURATE (UNII: I39GGJ23HV)
SODIUM GLYCOLATE (UNII: B75E535IMI)
SODIUM BENZOATE (UNII: OJ245FE5EU)
VACCINIUM ANGUSTIFOLIUM (BLUEBERRY) FRUIT (UNII: G90PX41VP0)
GLYCYRRHIZA GLABRA (LICORICE) ROOT (UNII: 2788Z9758H)
MELALEUCA ALTERNIFOLIA (TEA TREE) LEAF OIL (UNII: VIF565UC2G)
CITRIC ACID (UNII: 2968PHW8QP)
TRISODIUM DICARBOXYMETHYL ALANINATE (UNII: 784K2O81WY)
CHLORPHENESIN (UNII: I670DAL4SZ)
BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
ALGIN (UNII: C269C4G2ZQ)
WATER (UNII: 059QF0KO0R)
SODIUM CHLORIDE (UNII: 451W47IQ8X)
AZELAIC ACID (UNII: F2VW3D43YT)
GINGER (UNII: C5529G5JPQ)
DISODIUM 2-SULFOLAURATE (UNII: 329M3829G2)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 84126-237-50	50 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product	06/02/2025
2	NDC: 84126-237-18	1 in 1 CARTON	06/02/2025
2		180 mL in 1 BOTTLE, PUMP; 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	06/02/2025

Labeler - The Procter & Gamble Manufacturing Company (004238200)