Liquidproof
FDA Label NDC 78829-500
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Four Fathers Distillery Llc for the product Liquidproof (NDC 78829-500). 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 drug facts, otc - active ingredient, otc - purpose, indications & usage, warning, otc - keep out of reach of children, dosage & administration, other information:, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Otc - Active Ingredient
Active ingredient(s): Alcohol (ethanol) 70%.
Otc - Purpose
Purpose Antiseptic
Indications & Usage
Use(s): Helps reduce bacteria that can potentially become disease.
Warning
For external use only. FLAMMABLE: Keep away from heat and flame. DO NOT USE: On children less than 2 months of age. DO NOT USE: On open skin wounds. Keep out of eyes, ears, and mouth. Stop use if rash or irritation occurs. This could be a sign of a serious condition.
Otc - Keep Out Of Reach Of Children
Keep out of reach of children. If swallowed contact doctor or poison control right away.
Dosage & Administration
Directions: Place enough product on hands to cover all surfaces, rub together until dry. Supervise children under 6 years of age to prevent swallowing.
Other Information:
Store between 59-86°f. DO NOT store in heat above 105°f. May discolor some fabrics
Inactive Ingredient
Inactive ingredient(s): Glycerin, Aloe Barbadensis Leaf Juice, Hydroxyethylcellulose, Purified Water, Essential Oils
Packaging
Image (7882950081)
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