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  5. Label Information: Night Magic Roll-on Anti-perspirant Deodorant

FDA Label for Night Magic Roll-on Anti-perspirant Deodorant

View Indications, Usage & Precautions

Table of Contents

    1. OTC - ACTIVE INGREDIENT
    2. OTC - PURPOSE
    3. INDICATIONS & USAGE
    4. WARNINGS
    5. OTC - DO NOT USE
    6. DOSAGE & ADMINISTRATION
    7. INACTIVE INGREDIENT
    8. OTC - QUESTIONS
    9. PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Night Magic Roll-on Anti-perspirant Deodorant Product Label

The following document was submitted to the FDA by the labeler of this product New Avon Llc. The document includes published materials associated whith this product with the essential scientific information about this product as well as other prescribing information. Product labels may durg indications and usage, generic names, contraindications, active ingredients, strength dosage, routes of administration, appearance, warnings, inactive ingredients, etc.

Otc - Active Ingredient



Active ingredient

Aluminum Chlorohydrate 14.5%, anhydrous..


Otc - Purpose





Purpose

..Antiperspirant


Indications & Usage



Uses

•reduces underarm perspiration


Warnings



Warnings

For external use only


Otc - Do Not Use



Do not use on broken skin


Dosage & Administration



Directions

•apply to underarms only


Inactive Ingredient



Inactive ingredients

WATER/EAU, STEARETH-2, PPG-15 STEARYL ETHER, DICAPRYL ADIPATE, PARFUM/FRAGRANCE, STEARETH-20, ISOPROPYL PALMITATE


Otc - Questions



Questions?

Call 1-800-FOR-AVON or 1-800-265-AVON in Canada


Package Label.Principal Display Panel



image of label - PDP

image of label - PDP


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