INTELLIWRIST PERSONAL HAND SANITIZER- topical antiseptic liquid

Intelliwrist Personal Hand Sanitizer by

Drug Labeling and Warnings

Intelliwrist Personal Hand Sanitizer by is a Otc medication manufactured, distributed, or labeled by Intelwrist, LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredient(s)

Active Ingredient(s)

Ethyl acohol 70% v/v...................

Purpose

Purpose

Antiseptic

Use

Use

Hand sanitizer to help reduce bacteria on the skin that could cause disease.

Warnings

For external use only. Flammable. Keep away from heat or flame

Do not use

Do not use

• in children less than 2 months of age
• on open skin wounds

When using this product

When using this product keep out of eyes, ears and mouth. In case of contact with eyes, rinse eyes thoroughly with water.

Stop use and ask a doctor

Stop use and ask a doctor if irritation or rash occurs. These may be signs of a serious condition.

Keep out of reach of children.

Keep out of reach of children. If swallowed, get medical lhelp or contact a Poison Control Cernter right away.

Directions

Directions

• Place enough product on hands to cover all surfaces. Rub hands together until dry.
• Supervise children under 6 yeras of age when using this product to avoid swallowing.

Other Information

Other Information

• store between 15-30C (59-86F)
• Avoid freezing and excessive heat above 40C (104F)

Inactive Ingredients

Inactive Ingredients

water, glycerin, fragrance

PRINCIPAL DISPLAY PANEL

83135-001-01

PRINCIPAL DISPLAY PANEL

83135-001-02

INGREDIENTS AND APPEARANCE

INTELLIWRIST PERSONAL HAND SANITIZER 
topical antiseptic liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 83135-001
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	28 mL  in 40 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
GLYCERIN (UNII: PDC6A3C0OX)
FRAGRANCE 13576 (UNII: 5EM498GW35)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 83135-001-01	40 mL in 1 KIT; Type 0: Not a Combination Product	11/30/2022
2	NDC: 83135-001-02	40 mL in 1 BOX; Type 0: Not a Combination Product	11/30/2022

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	11/30/2022

Labeler - Intelwrist, LLC (008557500)