Active Ingredient
Aluminum Chlorohydrate 15%
La Fresh Hand Sanitizing Wipe
FDA Label NDC 64709-150
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Diamond Wipes International, Inc for the product La Fresh Hand Sanitizing Wipe (NDC 64709-150). 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, keep out of reach of children, directions, inactive ingredients, label, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Purpose
Antiperspirant
Use
reduce 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 kidney disease
Keep Out Of Reach Of Children
If swallowed, get medical help or contact a Poison Control Center right away
Directions
- open packet
- remove and unfold wipe
- apply to underarm only
Inactive Ingredients
Benzyl Alcohol, Fragrance, PEG-180, Phenoxyethanol, Polysorbate 20, Potassium Sorbate, Salvia Officinalis (Sage) Leaf Extract, Tocopherol, Tocopheryl Acetate, Usnea Barbata (Lichen) Extract, Water
Label
LA FRESH
travel lite
Antiperspirant Wipe
powerful wetness & odor protection
invisible, non-whitening formula
freshly scented
1 wipe 5.75" x 1.75" (14.6cm x 19.6 cm)
FSC FSC C109834 MIX Paper
RAINFOREST ALLIANCE CERTIFIED
For a refreshing getaway any day, Travel Lite and Live.Life.La Fresh
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Made in USA of foreign and domestic components
Distributed by La Fresh Group, Inc
Chino, CA 91710
www.LaFreshGroup.com
2015 La Fresh Group, Inc.
Item#F5324P PL-5324
UPC 766670053240
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