KIEHLS SINCE 1851 BLUE HERBAL ACNE CLEANSER TREATMENT- salicylic acid lotion

Kiehls Since 1851 Blue Herbal Acne Cleanser Treatment by

Drug Labeling and Warnings

Kiehls Since 1851 Blue Herbal Acne Cleanser Treatment 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 1.5%

Purpose

Acne treatment

Use

for the treatment of acne

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

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

Inactive ingredients

water, coco-glucoside, propylene glycol, ammonium polyacryloyldimethyl taurate, glycerin, coco-betaine, sodium cocoyl isethionate, sodium methyl cocoyl taurate, dipropylene glycol, sodium chloride, butylene glycol, phenoxyethanol, hydrogenated coconut acid, capryloyl salicylic acid, coconut acid, t-butyl alcohol, sodium PCA, camphor, menthol, boswellia serrata extract, sodium isethionate, hamamelis virginiana (witch hazel) water, peumus boldus leaf extract, disodium EDTA, alcohol, zingiber officinale (ginger) root extract, sanguisorba officinalis root extract, cinnamomum cassia bark extract, xanthan gum, laminaria saccharina extract, zinc sulfate, pyridoxine HCL, sodium hydroxide, citric acid

Questions or comments?

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PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

KIEHLS SINCE 1851 BLUE HERBAL ACNE CLEANSER TREATMENT 
salicylic acid lotion

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 49967-618
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ)	SALICYLIC ACID	15 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
COCO GLUCOSIDE (UNII: ICS790225B)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
GLYCERIN (UNII: PDC6A3C0OX)
COCO-BETAINE (UNII: 03DH2IZ3FY)
SODIUM COCOYL ISETHIONATE (UNII: 518XTE8493)
SODIUM METHYL COCOYL TAURATE (UNII: JVL98CG53G)
DIPROPYLENE GLYCOL (UNII: E107L85C40)
SODIUM CHLORIDE (UNII: 451W47IQ8X)
BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
CAPRYLOYL SALICYLIC ACID (UNII: 5F7PJF6AA4)
COCONUT ACID (UNII: 40U37V505D)
MENTHOL (UNII: L7T10EIP3A)
SODIUM ISETHIONATE (UNII: 3R36J71C17)
ALCOHOL (UNII: 3K9958V90M)
XANTHAN GUM (UNII: TTV12P4NEE)
ZINC SULFATE (UNII: 89DS0H96TB)
SODIUM HYDROXIDE (UNII: 55X04QC32I)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 49967-618-01	75 mL in 1 TUBE; Type 0: Not a Combination Product	03/01/2017
2	NDC: 49967-618-02	150 mL in 1 TUBE; Type 0: Not a Combination Product	03/01/2017
3	NDC: 49967-618-03	30 mL in 1 TUBE; Type 0: Not a Combination Product	03/01/2017
4	NDC: 49967-618-04	3 mL in 1 PACKET; Type 0: Not a Combination Product	03/01/2017

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph final	part333D	03/01/2017

Labeler - L'Oreal USA Products Inc (002136794)

Establishment
Name	Address	ID/FEI	Business Operations
L'Oreal USA, Inc.		185931458	manufacture(49967-618)