HAND SANITIZER LAVENDER 2OZ- alcohol liquid

Hand Sanitizer Lavender by

Drug Labeling and Warnings

Hand Sanitizer Lavender 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(s)

Ethyl Alcohol 70% v/v.

Purpose

Antimicrobial

Use

• for handwashing to decrease bacteria on the skin
• recommended for repeated use

Warnings

For external use only. Flammable, keep away from heat and 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 or rednees develp 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.

Directions

• Wet hands thoroughly with product
• briskly rub hands together until dry.
• Supervise children under 6 years of age when using this product.

Other information

• Store at room temperature
• may discolor certain fabrics

Inactive ingredients

water, carbomer, triethanolamine, glycerin, propylene glycol, fragrance, aloe barbadensis leaf juice, tocopheryl acetate, fd&c blue no. 1, fd&c red no.33.

QUESTIONS

1-855-345-5575

Package Label - Principal Display Panel

INGREDIENTS AND APPEARANCE

HAND SANITIZER LAVENDER  2OZ
alcohol liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 58503-155
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
FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
WATER (UNII: 059QF0KO0R)
TROLAMINE (UNII: 9O3K93S3TK)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
GLYCERIN (UNII: PDC6A3C0OX)
ALOE (UNII: V5VD430YW9)
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC)
ALPHA-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
D&C RED NO. 33 (UNII: 9DBA0SBB0L)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 58503-155-01	59 mL in 1 BOTTLE; Type 0: Not a Combination Product	09/30/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	09/28/2020

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

Establishment
Name	Address	ID/FEI	Business Operations
China Ningbo Shangge Technology Co., Ltd.		529287434	manufacture(58503-155)