FDA.reportPublic FDA data

Inixial Perfection STOP BLEMISHES Salicylic Acid 2% Acne Treatment Solution

Manufacturer
IXXI S.A.S
Effective date
2016-04-04
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
legacy-cache
Hydrated at
2026-08-02 01:27:43

Label at a glance#

ProductInixial Perfection STOP BLEMISHES Salicylic Acid 2% Acne Treatment
Active ingredientSALICYLIC ACID
Label structure7 sections

Indications and uses

For the treatment of acne. Dries and clears acne blemishes and allows skin to heal.

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. Sensitivity  Test f...

Label contents#

Full prescribing information#

Active ingredients

OTC - ACTIVE INGREDIENT SECTION

Salicylic acid 2%

Purpose

OTC - PURPOSE SECTION

Acne treatment solution

Uses

INDICATIONS & USAGE SECTION

  • For the treatment of acne.
  • Dries and clears acne blemishes and allows skin to heal.

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 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.

Sensitivity Test for a New User. Apply product sparingly to one or two small affected areas during the first 3 days. If no discomfort occurs, follow the directions stated above.

Inactive ingredients

INACTIVE INGREDIENT SECTION

water (aqua), SD alcohol 40-B, propanediol, citric acid, bamboo (Bambusa arundinacea) stem extract, cellulose, sodium hydroxide, polycrylate crosspolymer-6, alcohol, xanthan gum, glycerin, orris (Iris florentina) root extract, hydrogenated coconut acid, retinyl palmitate, zinc sulfate, sodium phytate, t-butyl alcohol, heather (Calluna vulgaris) flower extract, coco-caprylate/caprate, palmitoyl pine bark extract, palmitic acid.

Questions?

OTC - QUESTIONS SECTION

Call toll-free 1-800-322-3507

Package Labeling:

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

LabelLabel

Product Linked Resources#

Resource, Code type, Value table
ResourceCode typeValueEquivalent identifiersSource image
BarcodeEAN-133700677765246GTIN-13: 3700677765246
EAN-13: 3700677765246
GTIN storage (14 digits): 03700677765246		Label.jpg

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
70532-004-012026-01-06C16284748780-19d75b9cf-f362-f424-e053-dadaa90a57ceInixial Perfection STOP BLEMISHES Salicylic Acid 2% Acne Treatment Solution
70532-004-012020-01-31C16284748780-19d75b9cf-f362-f424-e053-dadaa90a57ceInixial Perfection STOP BLEMISHES Salicylic Acid 2% Acne Treatment Solution

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
70532-004INIXIAL PERFECTION STOP BLEMISHES SALICYLIC ACID 2% ACNE TREATMENT (SALICYLIC ACID) CREAM [IXXI S.A.S]2Legacy NDC20160404_28468efc-146b-4e7f-aa10-0bd0b5410fce.zip

Products#

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

DailyMed product names page 1 of 1 · 18 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
70532-00470532-004-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 17 matching rows.

Name, UNII, Kind table
NameUNIIKind
PALMITIC ACID2V16EO95H1IACT
SALICYLIC ACIDO414PZ4LPZACTIB
WATER059QF0KO0RIACT
PROPANEDIOL5965N8W85TIACT
CITRIC ACID MONOHYDRATE2968PHW8QPIACT
POWDERED CELLULOSESMD1X3XO9MIACT
SODIUM HYDROXIDE55X04QC32IIACT
ALCOHOL3K9958V90MIACT
XANTHAN GUMTTV12P4NEEIACT
GLYCERINPDC6A3C0OXIACT
IRIS PALLIDA ROOTLVV57EM5OGIACT
VITAMIN A PALMITATE1D1K0N0VVCIACT
ZINC SULFATE89DS0H96TBIACT
PHYTATE SODIUM88496G1ERLIACT
TERT-BUTYL ALCOHOLMD83SFE959IACT
CALLUNA VULGARIS FLOWERING TOPD9PC510CQVIACT
COCO-CAPRYLATE/CAPRATE8D9H4QU99HIACT

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
47b66f38-d80c-ecf6-e063-6394a90a41ca28468efc-146b-4e7f-aa10-0bd0b5410fce2026-01-06WarningsExact identifier
spl set id: 28468efc-146b-4e7f-aa10-0bd0b5410fce

Reported adverse events (FAERS/openFDA)#

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