Active Ingredient(S)
Benzalkonium Chloride 0.10% w/w. Purpose: Antiseptic
Hand Sanitizer
FDA Label NDC 77238-241
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Dgh Pharma, Inc. for the product Hand Sanitizer (NDC 77238-241). 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(s), purpose, use, warnings, otc - when using, otc - stop use, otc - keep out of reach of children, directions, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Purpose
Antiseptic, Hand Sanitizer
Use
Spray on mask and hands to sanitize & protect against bacteria and pathogens.
Warnings
For external use only.
Otc - When Using
When using this product keep out of eyes. In case of contact, flush eyes with water.
Stop use and ask a doctor if irritation or redness develops
Keep out of reach of children. If swallowed, get medical assistance or contact a Poison Control Center immediately.
Otc - Stop Use
Stop use and ask a doctor if irritation or redness develops.
Otc - Keep Out Of Reach Of Children
Keep out of reach of children. If swallowed, get medical assistance or contact a Poison Control Center immediately.
Directions
- Spray on hands and on each side of your mask
Inactive Ingredients
D-Limonene, Copper Chloide, Glycerin, Magnesium Hydroxide, PEG-8, PEG-90, Phenoxyethanol, Polysorbate 20, Purified Water, Trisodium Citrate
Package Label - Principal Display Panel
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