STEFANO

Manufacturer
ALL NATURAL DYNAMICS | Colgate Palmolive, S.A. de C.V.
Effective date
2022-03-21
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:48:52

Label at a glance#

ProductSTEFANO Black
Active ingredientALUMINUM CHLOROHYDRATE
Label structure8 sections

Dosage and administration

Apply under arm only. SHAKE WELL BEFORE USE.

Label contents#

Full prescribing information#

Active Ingredient:

OTC - ACTIVE INGREDIENT SECTION

ALUMINUM CHLOROHYDRATE 25%

Purpose:

OTC - PURPOSE SECTION

Antiperspirant

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep Out Of The Reach Of Children

USE:

INDICATIONS & USAGE SECTION

reduces underarm persperation.

Warnings:

WARNINGS SECTION

For External Use Only. Do Not Apply On Irritated Or Injured Skin. Discontinue Use If You Experience Some Irritation, Redness Or Discomfort.

Directions:

DOSAGE & ADMINISTRATION SECTION

Apply under arm only.

SHAKE WELL BEFORE USE.

Inactive Ingredients:

INACTIVE INGREDIENT SECTION

Water, Soy oil, stearth-2, PPG-15 stearyl ether, steareth-20, fragrance, caprylyl glycol, tetrasodium EDTA, and BHT

Stefano Black 50 mL

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Full LabelFull Label

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
51769-999-642022-05-06C16284748780-1de59bb17-5f2f-5c5e-e053-dadaa90a91d6STEFANO Black

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
51769-999-64STEFANOBlack50 g in 1 APPLICATORSTICK501

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
51769-999STEFANO BLACK (ALUMINUM CHLOROHYDRATE) STICK [ALL NATURAL DYNAMICS]1Legacy NDC, 1 package rows20220322_dabe3d86-4826-396c-e053-2a95a90ac338.zip

Products#

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

DailyMed product names page 1 of 1 · 9 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
51769-99951769-999-64

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 8 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
dabe3d86-4827-396c-e053-2a95a90ac338dabe3d86-4826-396c-e053-2a95a90ac3382022-03-21WarningsExact identifier
spl id: dabe3d86-4827-396c-e053-2a95a90ac338
spl set id: dabe3d86-4826-396c-e053-2a95a90ac338

Reported adverse events (FAERS/openFDA)#

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