HAND SANITIZER 1.8 OZ LEMON ICE- ethyl alcohol liquid

Hand Sanitizer 1.8 oz Lemon Ice by

Drug Labeling and Warnings

Hand Sanitizer 1.8 oz Lemon Ice 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

Hand sanitizer to help reduce bacteria on the skin that may cause disease

WARNINGS

For external use only.

Flammable, keep away from fire or flame

WHEN USING

When using this product

• avoid contact with face, eyes, and broken skin. In case of eye contact, flush with plenty of water and seek medical advice

STOP USE

Stop use and ask a doctor

• if irritation and redness develop

KEEP OUT OF REACH OF CHILDREN

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

DOSAGE & ADMINISTRATION

Directions

• Wet hands thoroughly with product and rub into skin until dry.
• Children under 6 years of age should be supervised by an adult when using

OTHER SAFETY INFORMATION

Other Information

• store at room temperature
• may discolor certain fabrics

INACTIVE INGREDIENT

water, carbomer, triethanolamine, glycerin, propylene glycol, fragrance, tocopheryl acetate (Vitamin E), aloe barbadensis leaf extract, fd&c yellow no. 5

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

HAND SANITIZER 1.8 OZ LEMON ICE 
ethyl alcohol liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 58503-124
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)
FD&C YELLOW NO. 5 (UNII: I753WB2F1M)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 58503-124-01	53 mL in 1 BOTTLE; Type 0: Not a Combination Product	04/03/2020

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(58503-124)