ULTRA DEFENSE SANI SMART HAND SANITIZER- alcohol spray 
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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Ultra Defense Sani Smart Hand Sanitizer Spray

Drug Facts

Active ingredient

Alcohol 69% v/v

Purpose

Antiseptic

Uses

Warnings

For external use only

Flammable, keep away from fire and flame.

When using this product

  • keep out of eyes. In case of contact with eyes, flush thoroughly with water.
  • avoid contact with broken skin
  • do not inhale or ingest

Stop use and ask a doctor if

  • irritation and redness develop and persist 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

Inactive ingredients

Water, Aloe Barbadensis Leaf Extract, Tocopheryl Acetate, Fragrance, Denatonium Benzoate.

Company Information

MANUFACTURED FOR & DISTRIBUTED BY K7 DESIGN GROUP LLC.

2433 KNAPP STREET, BROOKLYN, NY 11235

ORIGIN: CHINA

Product Packaging - 100 mL

100 ml

ULTRA DEFENSE SANI SMART HAND SANITIZER 
alcohol spray
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:74177-954
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL69 mL  in 100 mL
Inactive Ingredients
Ingredient NameStrength
WATER (UNII: 059QF0KO0R)  
ALOE VERA LEAF (UNII: ZY81Z83H0X)  
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)  
DENATONIUM BENZOATE (UNII: 4YK5Z54AT2)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:74177-954-01100 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product10/14/2020
2NDC:74177-954-029 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product10/14/2020
3NDC:74177-954-033 in 1 PACKAGE10/14/2020
39 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333A10/14/2020
Labeler - K7 Design Group Inc. (080357784)

Revised: 10/2020
Document Id: b2d38958-40ff-981d-e053-2a95a90a2fb3
Set id: b2d36b79-0934-3014-e053-2995a90a179a
Version: 1
Effective Time: 20201029
 
K7 Design Group Inc.