HAND SANITIZER- alcohol liquid 
K7 Design Group Inc.

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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K7 BBC Aloe Hand Sanitizer 62 Blstr

Active Ingredient

Alcohol Denat. 62%

Purpose

Antiseptic

Use

for hand-washing to help decrease bacteria on the skin, only when water is not available

Warnings

For external use only. Flammable, keep away from fire and flames.

When using this product

■ do not get into eyes.

■ if contact occurs, rinse eyes throughly with water.

Stop use and ask a doctor if

irritation and redness develops and persists.

Keep out of reach of children

if swallowed, get medical help or contact a Poison Control Center right away.

Directions

wet hands thoroughly with product and allow to dry without wiping

Inactive ingredients

Water, PEG-40 Hydrogenated Castor Oil, Fragrance, Acrylates/C10-30 Alkyl Acrylates Crosspolymer, Sodium Hydroxide, Aloe Barbadensis Leaf Juice, Denatonium Benzoate, Yellow 5, Blue 1

Inner Package Label

inner package label

Blister Package Label

outer package label

HAND SANITIZER 
alcohol liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:74177-028
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL62 mL  in 100 mL
Inactive Ingredients
Ingredient NameStrength
ALOE VERA LEAF (UNII: ZY81Z83H0X)  
GLYCERIN (UNII: PDC6A3C0OX)  
WATER (UNII: 059QF0KO0R)  
DENATONIUM BENZOATE (UNII: 4YK5Z54AT2)  
FD&C BLUE NO. 1 (UNII: H3R47K3TBD)  
POLYOXYL 40 HYDROGENATED CASTOR OIL (UNII: 7YC686GQ8F)  
SODIUM HYDROXIDE (UNII: 55X04QC32I)  
FD&C YELLOW NO. 5 (UNII: I753WB2F1M)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:74177-028-506 in 1 BLISTER PACK06/22/2020
1NDC:74177-028-0250 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333A06/22/2020
Labeler - K7 Design Group Inc. (080357784)

Revised: 7/2020
Document Id: a96896ac-03fd-8b5c-e053-2995a90aa26f
Set id: a968994f-f257-b79c-e053-2a95a90a0904
Version: 1
Effective Time: 20200703
 
K7 Design Group Inc.