HAND SANITIZER- alcohol gel 
Oingo Products LLC

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

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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

1893 mL NDC: 79436-101-06946 mL NDC: 79436-101-05236.5 mL NDC: 79436-101-03236.5 mL NDC: 79436-101-03

473 mL NDC: 79436-101-04473 mL NDC: 79436-101-04

HAND SANITIZER 
alcohol gel
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:79436-101
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL65 mL  in 100 mL
Inactive Ingredients
Ingredient NameStrength
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    
ShapeSize
FlavorImprint Code
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:79436-101-0410000 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product08/19/2020
2NDC:79436-101-0330000 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product08/19/2020
3NDC:79436-101-0510000 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product08/19/2020
4NDC:79436-101-0610000 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product08/19/2020
Image of Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333A03/30/2020
Labeler - Oingo Products LLC (117510957)
Registrant - Oingo Products LLC (117510957)

Revised: 8/2020
Document Id: ad2c1d6f-4b81-b1ad-e053-2a95a90a9c26
Set id: ad2c4ce6-0931-3cec-e053-2995a90a6d82
Version: 1
Effective Time: 20200818
 
Oingo Products LLC