FDA.reportPublic FDA data

Kiehls Since 1851 Blue Herbal Gel Cleanser Acne Treatment

Manufacturer
L'Oreal USA Products Inc | L'Oreal USA, Inc.
Effective date
2022-01-04
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
legacy-cache
Hydrated at
2026-08-01 22:19:28

Label at a glance#

ProductKiehls Since 1851 Blue Herbal Gel Cleanser Acne Treatment
Active ingredientSALICYLIC ACID
Label structure9 sections

Dosage and administration

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

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION


Salicylic acid 1.5%

Purpose

OTC - PURPOSE SECTION

Acne treatment

Use

INDICATIONS & USAGE SECTION

for the treatment of acne

Warnings

WARNINGS SECTION

For external use only

When using this product

OTC - WHEN USING SECTION

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.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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

Directions

DOSAGE & ADMINISTRATION SECTION

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

Inactive ingredients

INACTIVE INGREDIENT SECTION

water, coco-glucoside, propylene glycol, sorbitol, sodium laureth sulfate, treithanolamine, sodium chloride, PEG-120 methyl glucose dioleate, menthol, methylparaben, imidazolidinyl urea, benzophenone-4, disodium EDTA, dipropylene glycol, camphor, zinc PCA, aloe barbadensis leaf juice, boswella serrata extract, laminaria saccharina extract, blue 1, poterium officinale root extract, zinber officinale (ginger) root extract, cinnamomum cassia bark extract, hammamelis virginiana (witch hazel) leaf extract

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

image of a labelimage of a label

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 14 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
49967-61749967-617-01, 49967-617-02, 49967-617-03

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 13 matching rows.

Name, UNII, Kind table
NameUNIIKind
SALICYLIC ACIDO414PZ4LPZACTIB
WATER059QF0KO0RIACT
COCO-BETAINE03DH2IZ3FYIACT
PROPYLENE GLYCOL6DC9Q167V3IACT
SORBITOL506T60A25RIACT
SODIUM LAURETH SULFATEBPV390UAP0IACT
SODIUM CHLORIDE451W47IQ8XIACT
PEG-120 METHYL GLUCOSE DIOLEATEYM0K64F20VIACT
MENTHOLL7T10EIP3AIACT
METHYLPARABENA2I8C7HI9TIACT
DIPROPYLENE GLYCOLE107L85C40IACT
CAMPHOR (SYNTHETIC)5TJD82A1ETIACT
WITCH HAZEL101I4J0U34IACT

Source Document#

Source XML

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
bce0b2cf-f8e3-41ac-a149-aea517bb89d5effa0d12-65b5-48b7-a4eb-9177f58b25392023-01-27WarningsExact identifier
spl set id: effa0d12-65b5-48b7-a4eb-9177f58b2539

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.