WAVE HAND SANITIZER- alcohol gel

Wave Hand Sanitizer by

Drug Labeling and Warnings

Wave Hand Sanitizer by is a Otc medication manufactured, distributed, or labeled by C & A MARKETING, INC.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredient

Alcohol 75%v/v

Purpose

Antiseptic

Uses

■ Hand Sanitizer to help reduce bacteria on the skin. For use when soap and water are not available

Warnings

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

Do not use

■ on children less than 2 months of age ■ on open skin wounds

When using this product

keep out of eyes, ears, ears and mouth. In case of eye contact immediately flush eyes thoroughly with water

Stop use and ask a doctor

if irritation or rash occurs. These may be the signs of a serious condition.

Keep out of reach of children

In case of accidentail ingestion, contact a doctor or Poison Control Center immediately.

Directions

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

Other information

■ Store between 15º-30ºC (59º-89ºF) ■ Avoid freezing and excessive heat above 40ºC (104ºF) ■ May discolor fabrics or surfaces.

Inactive ingredients

■ Glycerin, hydroxypropyl cellulose, water

Package Label

INGREDIENTS AND APPEARANCE

WAVE HAND SANITIZER 
alcohol gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 78754-001
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)
HYDROXYPROPYL CELLULOSE, UNSPECIFIED (UNII: 9XZ8H6N6OH)
GLYCERIN (UNII: PDC6A3C0OX)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 78754-001-08	237 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	06/15/2020
2	NDC: 78754-001-16	500 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	06/15/2020
3	NDC: 78754-001-28	3790 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	06/15/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	06/15/2020

Labeler - C & A MARKETING, INC. (134723316)