Kiehls Since 1851 Blue Herbal Acne Spot Treatment

Manufacturer
L'Oreal USA Products Inc | L'Oreal USA, Inc. | Cosmetic Essence, LLC dba Voyant Beauty | Paklab
Effective date
2024-12-27
Label type
HUMAN OTC DRUG LABEL
Version
5
Source
legacy-cache
Hydrated at
2026-08-01 20:44:16

Label at a glance#

ProductKiehls Since 1851 Blue Herbal Acne Spot Treatment
Active ingredientSALICYLIC ACID
Label structure10 sections

Dosage and administration

clean the skin thoroughly before applying this product cover the entire affected area with a thin layer one to three times daily because excessive drying of the skin may occur, start with one application daily, then gradually ingrease to two or three times dialy if neded or as directed by a doctor if bothersome dryness or peeling occurs, reduce application to once a day or every other dayl

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION


Salicylic acid 2%

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

  • clean the skin thoroughly before applying this product
  • cover the entire affected area with a thin layer one to three times daily
  • because excessive drying of the skin may occur, start with one application daily, then gradually ingrease to two or three times dialy if neded or as directed by a doctor
  • if bothersome dryness or peeling occurs, reduce application to once a day or every other dayl

Inactive ingredients

INACTIVE INGREDIENT SECTION

water, alcohol denat., glycerin, butylene glycol, methyl methacrylate crosspolymer, ammonium polyacryloyldimethyl taurate, perlite, nylon-12, dipropylene glycol, xanthan gum, peumus boldus leaf extract, boswellia serrata extract, hamamelis virginiana (witch hazel) water, t-butyl alcohol, camphor, menthol, zingiber officinale (ginger) root extract, sanguisorba officinalis root extract, cinnamomum cassia bark extract, phenoxyethanol, cinnamal, laminaria accharina extract, zinc sulfate, pyridoxine HCL, sodium hydroxide, citric acid

Questions or comments?

OTC - QUESTIONS SECTION

Call toll-free 1-800-946-4453

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

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Products#

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NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
49967-52749967-527-01, 49967-527-02

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 27 matching rows.

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
7878e1c5-ace8-44a4-8c47-c27dce8e4190e74e09d1-ebef-4c44-9a11-c703a87a3c252024-12-27WarningsExact identifier
spl id: 7878e1c5-ace8-44a4-8c47-c27dce8e4190
spl set id: e74e09d1-ebef-4c44-9a11-c703a87a3c25

Reported adverse events (FAERS/openFDA)#

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