HAND SANITIZER 8 OZ. VITAMIN E 70 V/V- ethyl alcohol liquid

Hand Sanitizer 8 oz. Vitamin E by

Drug Labeling and Warnings

Hand Sanitizer 8 oz. Vitamin E by is a Otc medication manufactured, distributed, or labeled by China Ningbo Shangge Technology Co., Ltd.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Ethyl Alcohol 70.0% v/v

PURPOSE

Antimicrobial

INDICATIONS & USAGE

• For handwashing to decrease bacteria on the skin
• Recommended for repeated use

WARNINGS

For external use only.

Flammable, keep away from fire or flame.

Do not use in the eyes. In case of contact, rinse eyes thoroughly with water.

STOP USE

Stop use and ask a doctor if irritation and redness develop and persist for more than 72 hours.

KEEP OUT OF REACH OF CHILDREN

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

DOSAGE & ADMINISTRATION

• Wet hands thoroughly with product
• Briskly rub hands together until dry
• Supervise children under 6 years in the use of this product

OTHER SAFETY INFORMATION

Other Information

• store at room temperature
• may discolor certain fabrics

INACTIVE INGREDIENT

water, glycerin, carbomer, fragrance, triethanolamine, propylene glycol, tocopheryl acetate,

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

HAND SANITIZER 8 OZ. VITAMIN E  70 V/V
ethyl alcohol liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 58503-129
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	70 mL  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC)
TROLAMINE (UNII: 9O3K93S3TK)
GLYCERIN (UNII: PDC6A3C0OX)
WATER (UNII: 059QF0KO0R)
ALPHA-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
ALOE VERA LEAF (UNII: ZY81Z83H0X)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 58503-129-01	236 mL in 1 BOTTLE; Type 0: Not a Combination Product	03/05/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333E	03/05/2020

Labeler - China Ningbo Shangge Technology Co., Ltd. (529287434)

Establishment
Name	Address	ID/FEI	Business Operations
China Ningbo Shangge Technology Co., Ltd.		529287434	manufacture(58503-129)