Active Ingredient
Active Ingredient: Aluminum chlorohydrate 10%.
Kiwi Antiperspirant Deodorant Roll-on Cream
FDA Label NDC 84178-009
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Evi Labs for the product Kiwi Antiperspirant Deodorant Roll-on (NDC 84178-009). 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 active ingredient, purpose, use, warnings, instructions for use, inactive ingredients, indications & usage, directions, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Purpose
Antiperspirant
Use
Reduces underarm perspiration
Warnings
For external use only
Do not use on broken skin
Stop use if rash or irritation occurs
Ask a doctor before use if you have a kidney disease.
Keep of reach of children. If swallowed, get medical help or contact a Poison Control Center night away.
Instructions For Use
Shake well before use. Apply to underarms only. Close tight after use.
Inactive Ingredients
Fragrance, Poly aminopropyl Biguanide, PPG-15 Stearyl Ether, Steareth-2, Steareth-21, Water, Glycerin/ Actinidia Chinensis Fruit Extract/Sodium Benzoate/ Potassium Sorbate ( Fruit Ectract).
Indications & Usage
Do not use on broken skin.
Stop use if rash or irritation occurs.
Directions
SHAKE WELL BEFORE USE. APPLY TO UNDERARMS ONLY CLOSE TIGHT AFTER USE.
Otc - Keep Out Of Reach Of Children
Keep of reach of children. If swallowed, get medical help or contact
Poison Control Center night away.
* Please review the disclaimer below.
