Active Ingredient
Active Ingredient
Ethyl alcohol 60%
Sanitizer
FDA Label NDC 70143-1002
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Gandang Kalikasan Usa Inc. for the product Sanitizer (NDC 70143-1002). 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, uses:, purpose, warnings, otc - keep out of reach of children, directions, dosage & administration, inactive ingredients, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Uses:
Uses:
- Helps decrease bacteria on skin
- Recommended for repeated use
Purpose
Purpose
Antiseptic
Warnings
Warnings
For external use only. Avoid contact with eyes. If contact occurs, rinse with water.
Flammable, keep away from fire or flame.
Otc - Keep Out Of Reach Of Children
Keep out of reach of children. If swallowed, get medical help or contat a Poison Control Center right away.
For children under 6, use only under adult supervision. Not recommended for infants.
Directions
Directions:
Shake well.
Dosage & Administration
Spray onto hands and rub thorughly.
Inactive Ingredients
Inactive ingredients
aqua (water), Mentha piperita (peppermint) leaf essential oil, Mentha arvensis (corn mint) leaf essential oil, Aloe barbadensis leaf juice
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