KENDA CARE INSTANT HAND SANITIZER 70 PERCENT- ethyl alcohol gel

KENDA CARE INSTANT HAND SANITIZER by

Drug Labeling and Warnings

KENDA CARE INSTANT HAND SANITIZER by is a Otc medication manufactured, distributed, or labeled by MICRO CONNECTION ENTERPRISES INC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

ETHYL ALCOHOL 70% W/V

PURPOSE

ANTIMICROBIAL

USE

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

WARNINGS

For external use only. Flammable. Keep away from heat and flame. Do not inhale or ingest. Keep out of eyes, ears, and mouth. If eye contact occurs, flush thoroughly with water and seek medical advice. Avoid contact with broken skin. Not for use on infants. Stop use and ask a doctor if irritation, rash, or redness occurs. These may be signs of a serious condition.

KEEP OUT OF REACH OF CHILDREN

Keep out of reach of children. If swallowed, seek medical help or contact a Poison Control Center right away.

DIRECTIONS

• Dispense directly on hands and rub in thoroughly.
• Children under 6 should be helped and supervised.

OTHER INFORMATION

Store between 15°C and 37°C (59°F and 99°F). Avoid freezing. Avoid excessive heat above 40°C (104°F).

INACTIVE INGREDIENTS

Water, Glycerin, Aminomethyl Propanol, Acrylates/C10-30 Alkyl Acrylate Crosspolymer

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

KENDA CARE INSTANT HAND SANITIZER   70 PERCENT
ethyl alcohol gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 76038-404
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	70 mL  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
CARBOMER INTERPOLYMER TYPE A (ALLYL SUCROSE CROSSLINKED) (UNII: 59TL3WG5CO)
AMINOMETHYLPROPANOL (UNII: LU49E6626Q)
GLYCERIN (UNII: PDC6A3C0OX)
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 76038-404-17	500 mL in 1 BOTTLE; Type 0: Not a Combination Product	07/02/2020
2	NDC: 76038-404-10	300 mL in 1 BOTTLE; Type 0: Not a Combination Product	07/02/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333E	07/02/2020

Labeler - MICRO CONNECTION ENTERPRISES INC (144297160)