Otc - Active Ingredient
ACTIVE INGREDIENT
Benzalkonium Chloride - 0.26% (w/w)
Natrulab Antiseptic Sanitizing Wipes
FDA Label NDC 83086-001
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Natrulab Innovations Inc for the product Natrulab Antiseptic Sanitizing Wipes (NDC 83086-001). 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 otc - active ingredient, otc - purpose, indications & usage, warnings, otc - when using, otc - stop use, otc - keep out of reach of children, dosage & administration, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Otc - Purpose
Purpose
Antiseptic
Indications & Usage
USE
For hand washing to decrease bacteria on skin.
Recommended for repeated use.
Warnings
WARNINGS
For external use only
When using this product do not use in or near the eyes. In case of contact, rinse eyes thoroughly with water.
Stop use and ask a doctor if irritation or rash appears and lasts.
Keep out of reach of children. If swallowed, get medical help or contact a poison control center right away.
Otc - When Using
When using this product do not use in or near the eyes. In case of contact, rinse eyes thoroughly with water.
Otc - Stop Use
Stop use and ask a doctor if irritation or rash appears and lasts.
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.
Dosage & Administration
DIRECTIONS
Apply to clean dry hands. Wet hands thoroughly with the product and allow to dry. Children under 6 should be supervised when using this product.
Storage And Handling
OTHER INFORMATION
Do not store above 104℉ (40℃)
Do not use if the seal is damaged or broken
Inactive Ingredient
INACTIVE INGREDIENTS
Water, Sodium Hydroxymethylglycinate, Citric Acid, Aloe Barbadensis Leaf Water, Sodium Chloride, Sodium Benzoate, Potassium Sorbate
Package Label.Principal Display Panel
1000 COUNT REFILL BAG
NDC: 83086-001-01
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