FDA.reportPublic FDA data

Vichy Laboratoires Normaderm Phytoaction Daily Deep Cleansing

Manufacturer
COSMETIQUE ACTIVE PRODUCTION
Effective date
2020-04-16
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-01 23:35:17

Label at a glance#

ProductVichy Laboratoires Normaderm Phytoaction Daily Deep Cleansing
Active ingredientSalicylic Acid
Label structure9 sections

Dosage and administration

use twice daily wet face, 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

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

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

Inactive ingredients

INACTIVE INGREDIENT SECTION

water, coco-betaine, propanediol, PEG-120 methyl glyucose dioleate, sodium chloride, sodium cocoyl glycinate, dipropylene glycol, zinc gluconate, bifida ferment lysate, sodium hydroxide, sodium benzoate, phenoxyethanol, copper gluconate, caprylyl glycol, tetrasodium glutamate diacetate, fragrance

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

image of a labelimage of a label

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
69625-307-012024-01-31C16284748780-11030e365-586d-111a-e063-dadaa90a10e2Drug Facts
69625-307-022024-01-31C16284748780-11030e365-586d-111a-e063-dadaa90a10e2Drug Facts
69625-307-032024-01-31C16284748780-11030e365-586d-111a-e063-dadaa90a10e2Drug Facts
69625-307-042024-01-31C16284748780-11030e365-586d-111a-e063-dadaa90a10e2Drug Facts

Products#

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

DailyMed product names page 1 of 1 · 16 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
69625-30769625-307-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 15 matching rows.

Name, UNII, Kind table
NameUNIIKind
Salicylic AcidO414PZ4LPZACTIB
WATER059QF0KO0RIACT
COCO-BETAINE03DH2IZ3FYIACT
PROPANEDIOL5965N8W85TIACT
PEG-120 METHYL GLUCOSE DIOLEATEYM0K64F20VIACT
SODIUM CHLORIDE451W47IQ8XIACT
SODIUM COCOYL GLYCINATEXLU9KH03XMIACT
DIPROPYLENE GLYCOLE107L85C40IACT
ZINC GLUCONATEU6WSN5SQ1ZIACT
SODIUM HYDROXIDE55X04QC32IIACT
SODIUM BENZOATEOJ245FE5EUIACT
PHENOXYETHANOLHIE492ZZ3TIACT
COPPER GLUCONATERV823G6G67IACT
CAPRYLYL GLYCOL00YIU5438UIACT
TETRASODIUM GLUTAMATE DIACETATE5EHL50I4MYIACT

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
ce8dfde5-14a0-434f-8aaa-edc8a20745b13a0910c7-7672-419b-b8f2-c279f9ddcc7b2024-01-31WarningsExact identifier
spl set id: 3a0910c7-7672-419b-b8f2-c279f9ddcc7b

Reported adverse events (FAERS/openFDA)#

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