UHI HAND SANITIZER- hand sanitizer gel

UHI Hand Sanitizer by

Drug Labeling and Warnings

UHI Hand Sanitizer by is a Otc medication manufactured, distributed, or labeled by Kova Laboratories, Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredient(s)

Ethyl Alcohol 70% v/v

Purpose

Antiseptic, Hand Sanitizer

Use

For hand washing to decrease bacteria on the skin

Warnings

For external use only. Flammable. Do not use near heat, flame or while smoking.

Do not use

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

WHEN USING

When using this product keep out of eyes. if product gets into eyes, rinse with water to remove. Avoid contact with broken skin. Do not inhale or ingest.

STOP USE

Stop use and ask a doctor if rash or irritation develops and lasts.

KEEP OUT OF REACH OF CHILDREN

Keep out of reach of children. If swallowed, get medical help or contact a 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

Do not store above 104F

May discolor some fabrics, wood finishes, and plastics

Inactive ingredients

Water, Acrylates/C10-30 Alkyl Acrylate Crosspolymer, Propylene Glycol, Aloe Barbadensis Leaf Extract, PEG-8 Dimethicone, Triisopropanolamine, Linalool, FD&C Blue #1

UHI Hand Sanitizer

INGREDIENTS AND APPEARANCE

UHI HAND SANITIZER 
hand sanitizer gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 79417-020
Route of Administration	TOPICAL

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

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)	28.397 L  in 100 L
ALOE VERA LEAF (UNII: ZY81Z83H0X)	0.05 L  in 100 L
LINALOOL, (+/-)- (UNII: D81QY6I88E)	0.07 L  in 100 L
CARBOMER 1342 (UNII: 809Y72KV36)	0.27 L  in 100 L
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)	0.5 L  in 100 L
PEG-8 DIMETHICONE (UNII: GIA7T764OD)	0.3 L  in 100 L
TRIISOPROPANOLAMINE (UNII: W9EN9DLM98)	0.41 L  in 100 L
FD&C BLUE NO. 1 (UNII: H3R47K3TBD)	0.003 L  in 100 L

Product Characteristics
Color	blue (Translucent Gel)	Score
Shape		Size
Flavor		Imprint Code
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 79417-020-08	0.236 L in 1 BOTTLE, PUMP; Type 0: Not a Combination Product	07/28/2020
2	NDC: 79417-020-03	0.1 L in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product	07/28/2020
3	NDC: 79417-020-16	0.5 L in 1 BOTTLE, PUMP; Type 0: Not a Combination Product	07/28/2020
4	NDC: 79417-020-68	2 L in 1 JUG; Type 0: Not a Combination Product	07/28/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	07/28/2020

Labeler - Kova Laboratories, Inc. (193055027)

Registrant - Kova Laboratories, Inc. (193055027)

Establishment
Name	Address	ID/FEI	Business Operations
Kova Laboratories, Inc.		193055027	label(79417-020) , manufacture(79417-020)