ULTRA DEFENSE SANI SMART HAND SANITIZER- alcohol spray

Ultra Defense Sani Smart Hand Sanitizer by

Drug Labeling and Warnings

Ultra Defense Sani Smart Hand Sanitizer by is a Otc medication manufactured, distributed, or labeled by K7 Design Group Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Drug Facts

Active ingredient

Alcohol 69% v/v

Purpose

Antiseptic

Uses

• to decrease bacteria on the skin that could cause disease
• recommended for repeated use

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

• Spray directly on hands and rub in thoroughly
• For children under 6, use adult supervision
• Not recommended for infants

Other information

• Store between 15-30C (59-86F)
• Avoid freezing and excessive heat above 40C (104F)

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

INGREDIENTS AND APPEARANCE

ULTRA DEFENSE SANI SMART HAND SANITIZER 
alcohol spray

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 74177-954
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	69 mL  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
DENATONIUM BENZOATE (UNII: 4YK5Z54AT2)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 74177-954-01	100 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product	10/14/2020
2	NDC: 74177-954-02	9 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product	10/14/2020
3	NDC: 74177-954-03	3 in 1 PACKAGE	10/14/2020
3		9 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	10/14/2020

Labeler - K7 Design Group Inc. (080357784)