HAND SANITIZER LEMON SCENT HAND RX- ethyl alcohol gel

Hand Sanitizer Lemon Scent by

Drug Labeling and Warnings

Hand Sanitizer Lemon Scent by is a Otc medication manufactured, distributed, or labeled by Blue Cross Laboratories, Inc., Ningbo Liyuan Daily Chemical Products Co., Ltd.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Active ingredient              Purpose

Ethyl Alcohol  62.0%        Antimicrobial

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

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

Stop use and ask a doctor if irritation or redness develops

Warnings

For external use only

Flammable. Keep away from heat and flame.

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.

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 this product.

Inactive Ingredients water (aqua), triethanolamine, carbomer, aloe barbadensis leaf juice, fragrance, glycerin, propylene glycol, tocopheryl acetate (vitamin E).

PRINCIPAL DISPLAY PANEL

Hand Rx

Hand Sanitizer

Kills 99.99% of Germs

Leaves Hands Feeling Soft

Lemon Scent

2 FL OZ (59 mL)

INGREDIENTS AND APPEARANCE

HAND SANITIZER LEMON SCENT  HAND RX
ethyl alcohol gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 22431-132
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	62 g  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
TROLAMINE (UNII: 9O3K93S3TK)
CARBOMER HOMOPOLYMER TYPE B (ALLYL SUCROSE CROSSLINKED) (UNII: Z135WT9208)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
GLYCERIN (UNII: PDC6A3C0OX)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 22431-132-02	2 in 1 BLISTER PACK	08/19/2014
1	NDC: 22431-132-01	59 mL in 1 BOTTLE, PLASTIC; 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	part333E	08/19/2014

Labeler - Blue Cross Laboratories, Inc. (008298879)

Registrant - Blue Cross Laboratories, Inc. (008298879)

Establishment
Name	Address	ID/FEI	Business Operations
Ningbo Liyuan Daily Chemical Products Co., Ltd.		530766098	manufacture(22431-132)