Otc - Active Ingredient
ACTIVE INGREDIENT
Aluminum Chlorohydrate
Stefano Midnight
FDA Label NDC 69772-030
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Teresa Cecena Dba Genesis for the product Stefano Midnight (NDC 69772-030). This document serves as the official prescribing information, containing essential scientific data and clinical materials required for healthcare providers and patients.
This specific version of the label includes detailed information regarding otc - active ingredient, otc - purpose, otc - keep out of reach of children, dosage & administration, warnings, warnings and precautions, indications & usage, inactive ingredient, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Otc - Purpose
Purpose:
Antiperspirant
Otc - Keep Out Of Reach Of Children
Keep Out of reach of children
Dosage & Administration
Use:
REDUCES UNDERARM PERSPERATION
Warnings
FOR EXTERNAL USE ONLY
Warnings And Precautions
DO NOT APPLY ON IRRITATED OR IN JURED SKIN
DISCONTINUE USE IF YOU EXPERIENCE SOME IRRITATION, REDNESS OR DISCOMFORT.
Indications & Usage
APPLY UNDER ARM ONLY
SHAKE WELL BEFORE USE
Inactive Ingredient
WATER, SOY OIL, STEARTH-2, PPG-15 STEARYL ETHER, STEARETH-20,FRAGANCE,CAPRYLYLGLYCOL,TETRASOSIUM EDTA, AND BHT
Package Label.Principal Display Panel
Stefano Roll-on (Stefanomidnightrollon50ml)
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