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  4. 50636-004
  5. Label Information: Antiperspirant Deodorant

FDA Label for Antiperspirant Deodorant

View Indications, Usage & Precautions

Table of Contents

    1. ACTIVE INGREDIENT
    2. PURPOSE
    3. USES
    4. WARNINGS
    5. OTC - PREGNANCY OR BREAST FEEDING
    6. OTC - KEEP OUT OF REACH OF CHILDREN
    7. DIRECTIONS
    8. DRUG FACTS (CONTINUED) INACTIVE INGREDIENTS
    9. PACKAGE LABEL

Antiperspirant Deodorant Product Label

The following document was submitted to the FDA by the labeler of this product Frabel S.a De C.v.. 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.

Active Ingredient



Aluminum chlorohydrate 15%

Purpose



Antiperspirant

Uses



Reduces underarm perspiration

Warnings



For external use onlyDo not use on broken skin.Stop use if rash or irritation occurs.Ask a doctor before use if you have kidney disease

Otc - Pregnancy Or Breast Feeding



If pregnant or breast-feeding, ask a health professional before use.

Otc - Keep Out Of Reach Of Children



Keep out of reach of children. If swallowed get medical help or contact a Poison Control Center right away.


Directions



Apply to underarms only

Drug Facts (Continued) Inactive Ingredients



Water, corn starch, cetearyl alcohol, fragrance, hydroxycitronellal, eugenol, dimethicone, limonene, benzyl salcylate, linalool, cinnamyl alcohol, cinnamal,propylparaben, geraniol, ceteareth-33, methylparaben, EDTA, citronellol, hexyl cinnamal

Package Label



Package Label

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