Active Ingredients
Ethyl Alcohol 70% v/v
Rainwater
FDA Label NDC 76150-279
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Bell International Laboratories, Inc. for the product Rainwater (NDC 76150-279). 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 ingredients, purpose, uses, warnings, otc - keep out of reach of children, directions, other information, inactive ingredients, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Purpose
Antiseptic
Uses
To decrease bacteria on the skin
Recommended for repeated use
Warnings
For external use only
Flammable, keep away from fire or flame
Do not use in or near the eyes. In case of contact, rinse eyes thoroughly with water. Avoid contact with broken skin
Stop use and ask a doctor
- if irritation and redness develop
- Condition persists for more than 72 hours
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
Place enough product in your palm to thoroughly cover your hands
Children under 6 years of age should be supervised when using this product
Rub hands together briskly until dry
Other Information
Protect the product in this container from excessive heat and direct sun
Store below 104F (40C)
May discolor certain fabrics
Inactive Ingredients
Water, Aloe Barbadensis Leaf Juice, Leuconostoc/Radish Root Ferment Lysate Filtrate, Glycereth-26, Citrus Limon (Lemon) Peel Oil, Citrus Aurantifolia (Lime) Oil, Fragrance,
Label
Pouch (Rainwater Wwp)
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