UHI Hand Sanitizer

Manufacturer: Kova Laboratories, Inc.
Effective date: 2020-08-04
Label type: HUMAN OTC DRUG LABEL
Version: 2
Source: full-release
Hydrated at: 2026-05-31 23:23:58

Label at a glance#

ProductUHI Hand Sanitizer

Active ingredientALCOHOL

Label structure12 sections

Dosage and administration

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.

Storage and handling

Do not store above 104F May discolor some fabrics, wood finishes, and plastics

Label contents#

Full prescribing information#

Active Ingredient(s)

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol 70% v/v

Purpose

OTC - PURPOSE SECTION

Antiseptic, Hand Sanitizer

Use

INDICATIONS & USAGE SECTION

For hand washing to decrease bacteria on the skin

Warnings

WARNINGS SECTION

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

Do not use

OTC - DO NOT USE SECTION

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

OTC - WHEN USING SECTION

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.

OTC - STOP USE SECTION

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

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center immediately

Directions

DOSAGE & ADMINISTRATION SECTION

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

STORAGE AND HANDLING SECTION

Do not store above 104F

May discolor some fabrics, wood finishes, and plastics

Inactive ingredients

INACTIVE INGREDIENT SECTION

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

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

UHI 8 fl ozUHI 3 fl oz

16 oz

68 oz

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	SPL version
581662	ethanol 70 % Topical Gel	PSN	2
581662	ethanol 0.7 ML/ML Topical Gel	SCD	2
581662	ethanol 70 % Topical Gel	SY	2
581662	ethyl alcohol 70 % Topical Gel	SY	2

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
79417-020-03	2022-01-28	C162847	48780-1	d6a99b39-4411-a426-e053-dadaa90af4c2	278a51be-020d-485a-98af-75b1ec2a14dc
79417-020-08	2022-01-28	C162847	48780-1	d6a99b39-4411-a426-e053-dadaa90af4c2	278a51be-020d-485a-98af-75b1ec2a14dc
79417-020-16	2022-01-28	C162847	48780-1	d6a99b39-4411-a426-e053-dadaa90af4c2	278a51be-020d-485a-98af-75b1ec2a14dc
79417-020-68	2022-01-28	C162847	48780-1	d6a99b39-4411-a426-e053-dadaa90af4c2	278a51be-020d-485a-98af-75b1ec2a14dc

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	SPL version
79417-020-03	UHI Hand Sanitizer	0.1 L in 1 BOTTLE, DROPPER	GEL	0.1	2
79417-020-08	UHI Hand Sanitizer	0.236 L in 1 BOTTLE, PUMP	GEL	0.236	2
79417-020-16	UHI Hand Sanitizer	0.5 L in 1 BOTTLE, PUMP	GEL	0.5	2
79417-020-68	UHI Hand Sanitizer	2 L in 1 JUG	GEL	2	2

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
79417-020	UHI HAND SANITIZER (HAND SANITIZER) GEL [KOVA LABORATORIES, INC.]	2	Legacy NDC, 4 package rows	20200807_278a51be-020d-485a-98af-75b1ec2a14dc.zip

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 11 matching rows.

UHI Hand Sanitizer
Hand Sanitizer
WATER
ALOE VERA LEAF
LINALOOL, (+/-)-
CARBOMER 1342
PROPYLENE GLYCOL
PEG-8 DIMETHICONE
TRIISOPROPANOLAMINE
FD&C BLUE NO. 1
ALCOHOL

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
79417-020	79417-020-08, 79417-020-03, 79417-020-16, 79417-020-68

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 9 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
WATER	059QF0KO0R	IACT
ALOE VERA LEAF	ZY81Z83H0X	IACT
LINALOOL, (+/-)-	D81QY6I88E	IACT
CARBOMER 1342	809Y72KV36	IACT
PROPYLENE GLYCOL	6DC9Q167V3	IACT
PEG-8 DIMETHICONE	GIA7T764OD	IACT
TRIISOPROPANOLAMINE	W9EN9DLM98	IACT
FD&C BLUE NO. 1	H3R47K3TBD	IACT
ALCOHOL	3K9958V90M	ACTIB

Source Document#

Source XML

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
ac37c348-b397-1e05-e053-2995a90a8950			278a51be-020d-485a-98af-75b1ec2a14dc	2020-08-04	Warnings	Exact identifier spl id: ac37c348-b397-1e05-e053-2995a90a8950 spl set id: 278a51be-020d-485a-98af-75b1ec2a14dc

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.