KIEHLS GENTLY EFFECTIVE ACNE TREATING CLEANSING- salicylic acid paste

Kiehls Gently Effective Acne Treating Cleansing by

Drug Labeling and Warnings

Kiehls Gently Effective Acne Treating Cleansing by is a Otc medication manufactured, distributed, or labeled by L'Oreal USA Products Inc, L'OREAL USA, INC.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active ingredient

Salicylic acid 2%

Purpose

Acne treatment

Uses

• for the treatment of acne
• clears acne blemishes and allows skin to heal
• helps keep skin clear of new acne blemishes

Warnings

For external use only

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.

Keep out of reach of children.

If swallowed, get medical help or contact a Poison Control Center right away.

Directions

• use twice daily
• wet face, then work product into a lather
• massage onto face, avoiding the eyes
• rinse well

Inactive ingredients

water, glycerin, kaolin, sodium cocoyl isethionate, glyceryl stearate SE, cetyl alcohol, niacinamide, glycolipids, alpha-glucan oligosaccharide, carrageenan, beta-glucan, centella asiatica extract, ceramide NP, charcoal powder, chitosan, lactic acid, sodium benzoate, sodium hydroxide, trisodium ethylenediamine disuccinate

Questions or comments?

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PRINCIPAL DISPLAY PANEL

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PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

KIEHLS GENTLY EFFECTIVE ACNE TREATING CLEANSING 
salicylic acid paste

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 49967-464
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 mL

Inactive Ingredients
Ingredient Name	Strength
water (UNII: 059QF0KO0R)
glycerin (UNII: PDC6A3C0OX)
kaolin (UNII: 24H4NWX5CO)
sodium cocoyl isethionate (UNII: 518XTE8493)
glyceryl stearate SE (UNII: FCZ5MH785I)
cetyl alcohol (UNII: 936JST6JCN)
niacinamide (UNII: 25X51I8RD4)
alpha-glucan oligosaccharide (UNII: S95658MI3W)
carrageenan (UNII: 5C69YCD2YJ)
CENTELLA ASIATICA TRITERPENOIDS (UNII: 4YS74Q4G4J)
ceramide NP (UNII: 4370DF050B)
charcoal powder (UNII: 2P3VWU3H10)
POLIGLUSAM (UNII: 82LKS4QV2Y)
lactic acid (UNII: 33X04XA5AT)
sodium benzoate (UNII: OJ245FE5EU)
sodium hydroxide (UNII: 55X04QC32I)
trisodium ethylenediamine disuccinate (UNII: YA22H34H9Q)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 49967-464-01	125 mL in 1 TUBE; Type 0: Not a Combination Product	01/07/2025
2	NDC: 49967-464-02	1 in 1 CARTON	01/07/2025
2		15 mL in 1 TUBE; Type 0: Not a Combination Product
3	NDC: 49967-464-03	1 in 1 CARTON	03/18/2025
3		5 mL in 1 TUBE; Type 0: Not a Combination Product
4	NDC: 49967-464-04	2 mL in 1 PACKET; Type 0: Not a Combination Product	03/18/2025

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M006	01/07/2025

Labeler - L'Oreal USA Products Inc (002136794)

Establishment
Name	Address	ID/FEI	Business Operations
L'OREAL USA, INC.		185931458	manufacture(49967-464)