TRIDERMA MOISTURIZING HAND SANITIZER- alcohol gel

Triderma Moisturizing Hand Sanitizer by

Drug Labeling and Warnings

Triderma Moisturizing Hand Sanitizer by is a Otc medication manufactured, distributed, or labeled by Genuine Virgin Aloe Corporation. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active ingredient

Ethyl Alcohol 62% v/v

Purpose

Antimicrobial

Uses

​Hand sanitizer to help reduce bacteria on the skin that could cause disease. For use when soap and water are not available. Recommended for repeated use.

Warnings

Flammable, keep away from fire or flame.

For external use only

When using this product

keep out of eyes, ears and mouth. In case of contact rinse thoroughly with water. Avoid contact with broken skin.

Stop use and ask a doctor

if irritation or rash appears and lasts.

Keep out of reach of children.

If swallowed, get medical help or contact a Poison Control Center right away.

Directions

Place enough product in your palm to thoroughly cover your hands. Rub hands together until dry. For children under 6, use only under adult supervision. Not recommended for infants.

Other information

• Store below 105° F (40° C)
• May discolor certain fabrics or surfaces; harmful to wood finishes and plastics.

Inactive ingredients

deionized water, glycerin, isopropyl myristrate, aloe barbadensis leaf juice, tocopheryl acetate (vitamin E), crosspolymer

Questions?

1-800-279-7282 M-F 8am-4pm PST

Labels

Triderma MD ®

Moisturizing Hand Sanitizer

Kills 99% of Germs*

Helps reduce bacteria that could cause disease

Aloe & Vitamin E

Ethyl Alcohol

ANTIMICROBIAL

EXPERTS IN SKIN HEALING SINCE 1992

*Kills 99.9% of most common germs that may cause illness in as little as 15 seconds

Triderma.com

Dist. by: Genuine Virgin Aloe Corp.

Corona, CA 92879 ©2020

ITEM 173225 NDC: 10738-173-25

ITEM 173045 NDC: 10738-173-45

ITEM 173082 NDC: 10738-173-82

2.2 fl. oz. (65 ml)

4 fl. oz. (118 ml)

8 fl. oz. (236 ml)

INGREDIENTS AND APPEARANCE

TRIDERMA MOISTURIZING HAND SANITIZER 
alcohol gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 10738-173
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	0.62 mL  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
ALOE VERA LEAF (UNII: ZY81Z83H0X)
GLYCERIN (UNII: PDC6A3C0OX)
ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)
.ALPHA.-TOCOPHEROL ACETATE, DL- (UNII: WR1WPI7EW8)
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 10738-173-82	236 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product	05/01/2020
2	NDC: 10738-173-45	118 mL in 1 TUBE; Type 0: Not a Combination Product	05/01/2020
3	NDC: 10738-173-25	65 mL in 1 TUBE; Type 0: Not a Combination Product	05/01/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333E	05/01/2020

Labeler - Genuine Virgin Aloe Corporation (961374147)

Establishment
Name	Address	ID/FEI	Business Operations
Genuine Virgin Aloe Corporation		961374147	manufacture(10738-173)