FDA.reportPublic FDA data

Kiehls Since 1851 Blue Herbal Moisturizer Acne Treatment

Manufacturer
L'Oreal USA Products Inc | L'Oreal USA, Inc.
Effective date
2020-01-02
Label type
HUMAN OTC DRUG LABEL
Version
4
Source
legacy-cache
Hydrated at
2026-08-01 23:46:59

Label at a glance#

ProductKiehls Since 1851 Blue Herbal Moisturizer 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 0.5%

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, glycerin, montmorillonie, dimethicone, cyclohexasiloxane, glyceryl stearate SE, polyglyceryl-3 methylglycose distearate, stearyl alcohol, pentylene glycol, propylene glycol, methylparaben, chlorphenesin, xanthan gum, carbomer, sodium hydroxide, sodium PCA, butylparaben, dipropylene glycol, tetrasodium EDTA, laminaria saccharina extract, menthol, aloe barbadensis leaf juice, bosewella serrata extract, camphor, hammamelis virginiana (witch hazel) leaf extract, poterium officinale root extract, zinglber officinale (ginger) root extrct, cinnamomum cassia bark extract, blue 1

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

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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
49967-61649967-616-01, 49967-616-02

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
GLYCERINPDC6A3C0OXIACT
DIMETHICONE92RU3N3Y1OIACT
GLYCERYL STEARATE SEFCZ5MH785IIACT
CHLORPHENESINI670DAL4SZIACT
XANTHAN GUMTTV12P4NEEIACT
CARBOMER HOMOPOLYMER TYPE B (ALLYL PENTAERYTHRITOL OR ALLYL SUCROSE CROSSLINKED)K6MOM3T5YLIACT
SODIUM HYDROXIDE55X04QC32IIACT
BUTYLPARABEN3QPI1U3FV8IACT
DIPROPYLENE GLYCOLE107L85C40IACT
MENTHOL, UNSPECIFIED FORML7T10EIP3AIACT
CAMPHOR (NATURAL)N20HL7Q941IACT
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
fd43631a-dd54-4580-8f79-6c8d3f0bd5b48e1e86ca-c567-465b-9993-ddb5f97bb5f52021-12-30WarningsExact identifier
spl set id: 8e1e86ca-c567-465b-9993-ddb5f97bb5f5

Reported adverse events (FAERS/openFDA)#

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