HAND SANITIZER- alcohol spray 
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)

Alcohol 65% v/v. Purpose: Antiseptic

Purpose

Antiseptic, Hand Sanitizer

Use

for handwashing to decrease bacteria on the skin

Warnings

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

Do not use

When using this product

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

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

Package Label - Principal Display Panel

59 mL NDC: 79436-102-0159 mL NDC: 79436-102-01

HAND SANITIZER 
alcohol spray
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:79436-102
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)  
LAVENDER OIL (UNII: ZBP1YXW0H8)  
GLYCERIN (UNII: PDC6A3C0OX)  
Product Characteristics
Color    Score    
ShapeSize
FlavorImprint Code
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:79436-102-0140000 mL in 1 BOTTLE, SPRAY; 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 finalpart333A08/19/2020
Labeler - Oingo Products LLC (117510957)
Registrant - Oingo Products LLC (117510957)

Revised: 8/2020
Document Id: ad408102-be06-ca51-e053-2a95a90a5808
Set id: ad4075b3-7b42-6759-e053-2a95a90aed30
Version: 1
Effective Time: 20200819
 
Oingo Products LLC