LE VITAL BLOSSOM DELIGHT- ethyl alcohol gel

Le Vital Blossom Delight by

Drug Labeling and Warnings

Le Vital Blossom Delight by is a Otc medication manufactured, distributed, or labeled by Lantern Enterprises Ltd., Shanghai Lantern Cosmetic Co., Ltd.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Mecicical Ingredient

Ethyl Alcohol 62%

Purpose

Antiseptic

PURPOSE

Features

To decrease bacteria on the skin that could cause disease.

• Recommended for repeated use.
• Use anywhere without water.

KEEP OUT OF REACH OF CHILDREN

Keep out of reach of children. In case of accidental ingestion, seek professional assistance or contact a Poison Control Center immediately.

INDICATIONS & USAGE

Le Vital ® Signature

blossom delight

hand sanitizer 

DOSAGE & ADMINISTRATION

Directions

• Wet hands thoroughly with product and rub until dry without wiping
• For children under 6, use only under adult supervision.
• Not recommended for infants

WARNINGS

Warning

• For external use only - hands
• Flammable, keep away from heat and flame
• Discontinue if skin becomes irritated and ask a doctor

CAUTION: For external use only. This product was not tested on animals.

When using this product

• Keep out of eyes. In case of contact with eyes, flush thoroughly with water.
• Do not inhale or ingest.
• Avoid contact with broken skin.

Other information

• Do not store above 105°F.
• May discolor some fabrics.
• Harmful to wood finishes and plastics.

INACTIVE INGREDIENT

Non-Medicinal

water, isopropyl alcohol, glycerin, carbomer, aminomethyl propanol, parfum, propylene glycol, isopropyl myristate, aloe barbadensis leaf juice, tacopheryl acetate

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

LE VITAL BLOSSOM DELIGHT 
ethyl alcohol gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 50154-003
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 g

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
ISOPROPYL ALCOHOL (UNII: ND2M416302)
GLYCERIN (UNII: PDC6A3C0OX)
CARBOMER COPOLYMER TYPE A (UNII: 71DD5V995L)
AMINOMETHYLPROPANOL (UNII: LU49E6626Q)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 50154-003-01	29 g in 1 PACKAGE; 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	07/23/2015

Labeler - Lantern Enterprises Ltd. (004005196)

Establishment
Name	Address	ID/FEI	Business Operations
Shanghai Lantern Cosmetic Co., Ltd.		421252043	manufacture(50154-003)