Active Ingredient(S)
Alcohol 75% v/v. Purpose: Antiseptic
Suppress Hand Sanitizer
FDA Label NDC 77343-111
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Hd Group Llc for the product Suppress Hand Sanitizer (NDC 77343-111). 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, do not use, otc - when using, otc - stop use, otc - keep out of reach of children, 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
to decrease bacteria on the skin.
Warnings
For external use only. Do not inhale or ingest. Flammable. Keep away from heat or flame when using this product.
Do Not Use
- in children less than 2 months of age
- on open skin wounds
Otc - When Using
When using this product keep away from eyes. In case of contact with eyes, flush thoroughly with water. Avoid contact with broken skin.
Otc - Stop Use
Stop use and ask a physician if skin irritation occurs.
Otc - Keep Out Of Reach Of Children
Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center immediately.
Directions
- Apply to hands thoroughly and rub vigorously until dry.
- For children under 6 years, use only with adult supervision.
- Not recommended for infants.
Other Information
- Do not store above 104F (40C)
- May discolor some fabrics
- harmful to some wood finishes
Inactive Ingredients
purified water USP
PEG-40 hydrogenated castor oil
carbomer
sodium hydroxide
aloe vera extract
Package Label - Principal Display Panel
500 mL NDC: 77343-111-01
Distributed By:
Distributed by: HD Group LLC 335 N Edgewood Ln, Suite 130 Eagle, ID 83616
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