DR. TALBOTS- ethyl alcohol gel

Dr. Talbots by

Drug Labeling and Warnings

Dr. Talbots by is a Otc medication manufactured, distributed, or labeled by Talbot’s Pharmaceuticals Family Products, LLC.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Purpose

Antiseptic, Hand Sanitizer

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

WHEN USING

When using this product avoid contact with eyes. If contact occurs, rinse thoroughly with water.

STOP USE

Stop use and ask a doctor if irritation or redness develops, condition persists for more than 72 hours consult a doctor.

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

ACTIVE INGREDIENT

Ethyl Alcohol 75%

Package Label - Principal Display Panel

INGREDIENTS AND APPEARANCE

DR. TALBOTS 
ethyl alcohol gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 70797-160
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	75 mL  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
AMINOMETHYL PROPANEDIOL (UNII: CZ7BU4QZJZ)
CARBOMER 934 (UNII: Z135WT9208)
GLYCERIN (UNII: PDC6A3C0OX)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 70797-160-01	50 mL in 1 BOTTLE; Type 0: Not a Combination Product	05/29/2020
2	NDC: 70797-160-02	250 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product	05/29/2020
3	NDC: 70797-160-03	500 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product	05/29/2020
4	NDC: 70797-160-04	1000 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product	05/29/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	05/29/2020

Labeler - Talbot’s Pharmaceuticals Family Products, LLC. (078855555)