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Drug Facts
Premium Hand Sanitizer
FDA Label NDC 69898-501
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Md Science Lab Llc for the product Premium Hand Sanitizer (NDC 69898-501). 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 other, active ingredient, purpose, use, warnings, 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
Active Ingredient
Benzalkonium Chloride 0.13%
Purpose
Antimicrobial
Use
- For hand sanitizing to decrease bacteria on the skin
- Recommended for repeated use
Warnings
- For external use only.
Otc - When Using
- When using this product avoid contact with eyes. In case of eye contact, flush eyes with water.
Otc - Stop Use
- Stop use and a ask doctor if irritation or redness develops, or if 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
- Pump a small amount of liquid into palm of hand.
- Rub thoroughly over all surfaces of both hands.
- Rub hands together briskly until dry.
Inactive Ingredients
Water (aqua), Propylene Glycol, Polysorbate 20, Phenoxyethanol, Melaleuca Alternifolia (Tea Tree) Leaf Oil, Lavandula Angustifolia (Lavender) Oil, Aloe barbadensis (Aloe Vera).
Principal Display Panel - 237 Ml Bottle Label
M.D.
Science Lab
LLC
PREMIUM
hand
sanitizer
with Tea Tree Oil & Aloe
Kills 99.99% of Germs
Antimicrobial - Alcohol Free
moisturizes & softens skin
8 fl oz 237ml e
Principal Display Panel (237 ml Bottle Label)
* Please review the disclaimer below.
