FDA.reportPublic FDA data

Vichy Laboratoires Normaderm Acne Control Moisturizer

Manufacturer
COSMETIQUE ACTIVE PRODUCTION
Effective date
2023-12-11
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-06-01 00:03:49

Label at a glance#

ProductVichy Laboratoires Normaderm Acne Control Moisturizer
Active ingredientSalicylic Acid
Label structure11 sections

Indications and uses

for the treatment of acne clears acne blemishes and allows skin to heal helps prevent new acne blemishes

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 increase to two or three times daily if needed or as directed by a doctor • if bothersome dryness or peeling occurs, reduce application to once a day or every other day

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Salicylic acid...2%

Purpose

OTC - PURPOSE SECTION

Acne treatment

Uses

INDICATIONS & USAGE SECTION

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

Warnings

WARNINGS SECTION

For external use only

Flammable until dry.

USER SAFETY WARNINGS SECTION

Keep away from flames and heat.

When using this product

OTC - WHEN USING SECTION

kin 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 increase to two or three times daily if needed or as directed by a doctor
• if bothersome dryness or peeling occurs, reduce application to once a day or every other day

Inactive ingredients

INACTIVE INGREDIENT SECTION

water, glycerin, butylene glycol, isononyl isononanoate, kaolin, hydrolyzed algin, zinc sulfate, bifida ferment lysate, sarcosine, sodium hyaluronate, sodium hydroxide, trisodium ethylenediamine disuccinate, ascorbyl glucoside, acetic acid, acrylates/c10-30 alkyl acrylate crosspolymer, biosaccharide gum-1, caprylyl glycol, lactic acid, maltodextrin, pentylene glycol, sodium polyacrylate, xanthan gum, sodium benzoate, fragrance

Questions or comments?

OTC - QUESTIONS SECTION

Call toll free 1-877-378-4249

Monday - Friday (9 a.m. to 5 p.m. EST)

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

image of a cartonimage of a carton

image of a carton
image of a carton

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
346298salicylic acid 2 % Topical GelPSN2
346298salicylic acid 0.02 MG/MG Topical GelSCD2
346298salicylic acid 2 % Topical GelSY2

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
c6f86816-7da6-43ea-8c25-ac9758311cc5Product name120220118
3c386306-c48a-413e-bb69-70cb268496f3Product name120210727
f52be47f-7aa7-46c0-b1fa-50c18dd50206Product name120201029
444b3e50-f226-46ef-bfca-2e7035d140cdProduct name120190611
dea2eded-d1e7-46bb-9a3d-f8dc20de6277Product name120190408
7cda52fc-125f-421c-8fea-bc1974370c49Product name220180703
48747306-602a-42cc-957b-5b0c69158eeeProduct name120180604
252e11b6-1a9a-4283-a242-df2c129c496dProduct name320170717
597b1cfd-7b31-5048-62be-ca5cd740da2fProduct name120140508
db5ebcdb-b6ae-21cd-4dc5-76cd84b5578bProduct name120140508
ec2149b3-5c6d-5344-f757-c86411073075Product name120140508

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
69625-661-01Vichy Laboratoires Normaderm Acne Control Moisturizer1 in 1 CARTONGEL12
69625-661-01Vichy Laboratoires Normaderm Acne Control Moisturizer50 mL in 1 BOTTLEGEL502

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
69625-661VICHY LABORATOIRES NORMADERM ACNE CONTROL MOISTURIZER (SALICYLIC ACID) GEL [COSMETIQUE ACTIVE PRODUCTION]2Current NDC, 2 package rows20231212_04df2f5d-77f0-4553-9d8c-3f10628736ae.zip

Products#

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

DailyMed product names page 1 of 1 · 22 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
69625-66169625-661-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 21 matching rows.

Name, UNII, Kind table
NameUNIIKind
Salicylic AcidO414PZ4LPZACTIB
WATER059QF0KO0RIACT
GLYCERINPDC6A3C0OXIACT
ISONONYL ISONONANOATES4V5BS6GCXIACT
BUTYLENE GLYCOL3XUS85K0RAIACT
KAOLIN24H4NWX5COIACT
ZINC SULFATE89DS0H96TBIACT
SARCOSINEZ711V88R5FIACT
HYALURONATE SODIUMYSE9PPT4THIACT
SODIUM HYDROXIDE55X04QC32IIACT
TRISODIUM ETHYLENEDIAMINE DISUCCINATEYA22H34H9QIACT
ASCORBYL GLUCOSIDE2V52R0NHXWIACT
ACETIC ACIDQ40Q9N063PIACT
BIOSACCHARIDE GUM-1BB4PU4V09HIACT
CAPRYLYL GLYCOL00YIU5438UIACT
LACTIC ACID33X04XA5ATIACT
MALTODEXTRIN7CVR7L4A2DIACT
PENTYLENE GLYCOL50C1307PZGIACT
SODIUM POLYACRYLATE (2500000 MW)05I15JNI2JIACT
XANTHAN GUMTTV12P4NEEIACT
SODIUM BENZOATEOJ245FE5EUIACT

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
Vichy Laboratoires Normaderm Acne Control MoisturizerSALICYLIC ACIDCOSMETIQUE ACTIVE PRODUCTION04df2f5d-77f0-4553-9d8c-3f10628736ae2023-12-11WarningsExact identifier
ndc (package): 69625-661-01
ndc (product): 69625-661
ndc11 (package): 69625066101
spl id: 34aa8648-77df-491b-ad70-c44b075921d4
spl set id: 04df2f5d-77f0-4553-9d8c-3f10628736ae

Reported adverse events (FAERS/openFDA)#

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