Purpose
Antiseptic, Hand Sanitizer
Purpose (16030 Dt)
Dr. Talbots Gel
FDA Label NDC 70797-160
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Talbot�s Pharmaceuticals Family Products, Llc. for the product Dr. Talbots (NDC 70797-160). 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 purpose, use, warnings, otc - when using, otc - stop use, otc - keep out of reach of children, directions, other information, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Use
To help reduce bacteria on the skin that could cause disease. Recommended for repeated use.
Warnings
For external use only. Flammable. Keep away from heat or flame
Otc - When Using
When using this product avoid contact with eyes. If contact occurs, rinse thoroughly with water.
Otc - Stop Use
Stop use and ask a doctor if irritation or redness develops, condition persists for more than 72 hours consult a doctor.
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
- Wet hands thoroughly with product and allow to dry without wiping.
- For children under 6, use only under adult supervision.
Other Information
- Store at normal room temperature
- May discolor certain fabrics
- May be harmful to wood finishes and plastics
Inactive Ingredients
aqua, glycerin, carbomer, aminomethyl propanol
Otc - Active Ingredient
Ethyl Alcohol 75%
Package Label - Principal Display Panel
Principal Display Panel (16026 Dt)
Principal Display Panel (16032)
Principal Display Panel (16031 Dt)
Purpose (16030 Dt)
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