Personox Ultimate Scrub Cleanser

Manufacturer
Stonebridge Consultants LLC | Southeast Holdings Corp
Effective date
2025-11-12
Label type
HUMAN OTC DRUG LABEL
Version
4
Source
full-release
Hydrated at
2026-06-01 01:43:27

Label at a glance#

ProductPersonox Ultimate Scrub Cleanser
Active ingredientSALICYLIC ACID
Label structure9 sections

Indications and uses

FOR THE TREATMENT OF ACNE

Dosage and administration

CLEANSE UP TO TWICE A DAY OR AS INSTRUCTED BY A PHYSICIAN. WET FACE, APPLY A SMALL AMOUNT OF PRODUCT TO WET HANDS AND WORK INTO A LATHER ON AREAS TO BE TREATED - MASSAGE GENTLY, RINSE THOROUGHLY.

Storage and handling

STORE IN A COOL DRY PLACE DO NOT FREEZE

Label contents#

Full prescribing information#

ACTIVE INGREDIENT

OTC - ACTIVE INGREDIENT SECTION

SALICYLIC ACID.......... 1.5% W/W

PURPOSE

OTC - PURPOSE SECTION

ACNE TREATMENT

USES

INDICATIONS & USAGE SECTION

FOR THE TREATMENT OF ACNE

WARNINGS

WARNINGS SECTION

FOR EXTERNAL USE ONLY

WHEN USING THIS PRODUCT

  • AVOID CONTACT WITH EYES AND MOUTH. IF CONTACT OCCURS, RINSE THOROUGHLY WITH WATER.
  • 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 MEDICATION AT A TIME.
  • LIMIT USE TO FACE AND NECK.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

KEEP OUT OF REACH OF CHILDREN.

IF PRODUCT IS SWALLOWED, GET MEDICAL HELP OR CONTACT A POISON CONTROL CENTER RIGHT AWAY.

DIRECTIONS

DOSAGE & ADMINISTRATION SECTION

CLEANSE UP TO TWICE A DAY OR AS INSTRUCTED BY A PHYSICIAN. WET FACE, APPLY A SMALL AMOUNT OF PRODUCT TO WET HANDS AND WORK INTO A LATHER ON AREAS TO BE TREATED - MASSAGE GENTLY, RINSE THOROUGHLY.

INACTIVE INGREDIENTS

INACTIVE INGREDIENT SECTION

WATER, SILICA DIOXIDE, COCO-GLUCOSIDE, SODIUM ISETHIONATE, POLOXAMER 184, SODIUM DIOCTYL SULFOSUCCINATE, SODIUM DODECYLBENZENESULFONATE, SULFUR, CORN STARCH, CELLULOSE GUM, FRAGRANCE, TETRASODIUM EDTA, MAGNESIUM ALUMINUM SILICATE

OTHER INFORMATION

STORAGE AND HANDLING SECTION

  • STORE IN A COOL DRY PLACE
  • DO NOT FREEZE

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Front LabelFront LabelBack LabelBack Label

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1234456salicylic acid 1.5 % Medicated Liquid SoapPSN4
1234456salicylic acid 15 MG/ML Medicated Liquid SoapSCD4
1234456salicylic acid 1.5 % Medicated Liquid SoapSY4

Product Linked Resources#

Resource, Code type, Value table
ResourceCode typeValueEquivalent identifiersSource image
BarcodeEAN-130196852702107GTIN-13: 0196852702107
EAN-13: 0196852702107
GTIN-12: 196852702107
UPC-A: 196852702107
GTIN storage (14 digits): 00196852702107
01b LBL-front_Personox Scrub_4oz.jpg

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
dea2eded-d1e7-46bb-9a3d-f8dc20de6277Product name120190408

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
83044-101-04Personox Ultimate Scrub Cleanser120 g in 1 BOTTLECREAM1204

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
83044-10183044-101-04

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 13 matching rows.

Source Document#

Source XML

Older Hydrated Versions#

Version, Effective date, Source table
VersionEffective dateSourceHydrated
22025-01-15full-release2026-06-01 00:52:48

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
Personox Ultimate Scrub CleanserSALICYLIC ACIDStonebridge Consultants LLC2b8b5134-ad05-3345-e063-6294a90a87512025-11-12WarningsExact identifier
ndc (package): 83044-101-04
ndc (product): 83044-101
ndc11 (package): 83044010104
spl id: 436d3ec8-77e3-8cd2-e063-6294a90a18fc
spl set id: 2b8b5134-ad05-3345-e063-6294a90a8751

Reported adverse events (FAERS/openFDA)#

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