ASTRAL ORGANICA HAND SANITIZER- hand santizer gel

Astral Organica Hand Sanitizer by

Drug Labeling and Warnings

Astral Organica Hand Sanitizer by is a Otc medication manufactured, distributed, or labeled by Kabana Skin Care. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

PRINCIPAL DISPLAY PANEL

Package Insert - label is too small for Drug Facts Table

Astral Organica Hand Sanitizer Label - note QR Code referencing Drug Facts for easy access via smart device.

ACTIVE INGREDIENT

ETHYL ALCOHOL 70% V/V

PURPOSE

ANTIMICROBIAL

WHEN USING THIS PRODUCT, DO NOT USE IN OR NEAR THE EYES. IN CASE OF CONTACT, RINSE EYES THOROUGHLY WITH WATER.

DISCONTINUE USE IF IRRITATION OR REDNESS DEVELOPS.

IF CONDITION PERSISTS FOR MORE THAN 72 HOURS, CONSULT A DOCTOR.

KEEP OUT OF REACH OF CHILDREN. IF SWALLOWED, GET MEDICAL HELP OR CONTACT A POISON CENTER RIGHT AWAY.

USE

HAND SANITIZER TO HELP REDUCE PATHOGENS ON THE SKIN

WARNINGS

FLAMMABLE. KEEP AWAY FROM FIRE OR FLAME.

THIS PRODUCT IS INTENDED FOR EXTERNAL USE ONLY.

DIRECTIONS

• PLACE ENOUGH PRODUCT IN YOUR PALM TO THOROUGHLY COVER YOUR HANDS
• RUB HANDS TOGETHER BRISKLY UNITL DRY
• CHILDREN UNDER 6 YEARS OF AGE SHOULD BE SUPERVISED WHEN USING THIS PRODUCT

OTHER INFORMATION

• STORE BELOW 110oF (44oC)
• MAY DISCOLOR CERTAIN FABRICS OR SURFACES

INACTIVE INGREDIENTS

WATER (AQUA), HYDROXYETHYLCELLULOSE

INGREDIENTS AND APPEARANCE

ASTRAL ORGANICA HAND SANITIZER 
hand santizer gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 73369-0010
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	64.7 g  in 100 g

Inactive Ingredients
Ingredient Name	Strength
HYDROXYETHYL CELLULOSE, UNSPECIFIED (UNII: T4V6TWG28D)	1.2 g  in 100 g
WATER (UNII: 059QF0KO0R)	34.1 g  in 100 g

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 73369-0010-1	43.4 g in 1 BOTTLE, PUMP; Type 0: Not a Combination Product	08/02/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	505G(a)(3)	08/02/2020

Labeler - Kabana Skin Care (080237112)

Registrant - Kabana Skin Care (080237112)

Establishment
Name	Address	ID/FEI	Business Operations
Kabana Skin Care		080237112	manufacture(73369-0010)