HAND SANITIZER- alcohol gel

Hand Sanitizer by

Drug Labeling and Warnings

Hand Sanitizer by is a Otc medication manufactured, distributed, or labeled by Oingo Products LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredient(s)

Ethyl Alcohol 62.5% v/v…………………..……... Antiseptic

Use

Hand Sanitizer to help reduce bacteria that potentially can cause disease. For use when soap and water are not available.

Warnings

For external use only | Flammable, keep away from fire or flame, heat, sparks, and sources of static discharge

Do not use

In eyes | on children less than 2 months of age | on open skin wounds

When Using

If in eyes, rinse promptly and thoroughly with water | Discontinue use if irritation and redness Develops

Stop use and ask a doctor

if skin irritation or redness occurs

or persists for more than 72 hours.

Keep out of reach of children.

If swallowed, get medical help

or contact a Poison Control Center right away.

Directions

Apply product onto hands, spread thoroughly and

rub dry | Supervise children under 6 years of age when using

this product to avoid swallowing.

Other information

Other Information For additional information, see Safety Data

Sheets (SDS) | For emergency medical information in USA and

Canada, call 1-888-255-3924 | Store between 15-

30C (59-86F) | Avoid freexing and excessive heat above 40C

(104F)

​

Inactive ingredients

water (aqua), propylene glycol,

dimethicone PEG-7 Isostearate, acrylates/ C10-30 Alkyl

Acrylate Crosspolymer, aminomethylpropanediol, tocopherol

acetate, aloe barbadensis leaf juice

Purpose

​Antiseptic, Hand Sanitizer

Package Label - Principal Display Panel

236.5 mL NDC: 79436-101-03

473 mL NDC: 79436-101-04

INGREDIENTS AND APPEARANCE

HAND SANITIZER 
alcohol gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 79436-101
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	65 mL  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
ALOE (UNII: V5VD430YW9)
AMINOMETHYL PROPANEDIOL (UNII: CZ7BU4QZJZ)
PPG-14 BUTYL ETHER (UNII: R199TJT95T)
.ALPHA.-TOCOPHEROL ACETATE, D- (UNII: A7E6112E4N)
CARBOMER INTERPOLYMER TYPE A (55000 CPS) (UNII: 59TL3WG5CO)
DIMETHICONE PEG-7 ISOSTEARATE (UNII: JVS3399FNW)

Product Characteristics
Color		Score
Shape		Size
Flavor		Imprint Code
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 79436-101-04	10000 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	08/19/2020
2	NDC: 79436-101-03	30000 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product	08/19/2020
3	NDC: 79436-101-05	10000 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product	08/19/2020
4	NDC: 79436-101-06	10000 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product	08/19/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	03/30/2020

Labeler - Oingo Products LLC (117510957)

Registrant - Oingo Products LLC (117510957)