MELLOW INSTANT HAND SANITIZER ORIGINAL- ethyl alcohol gel

Mellow Instant Hand Sanitizer Original by

Drug Labeling and Warnings

Mellow Instant Hand Sanitizer Original by is a Otc medication manufactured, distributed, or labeled by Lantern Enterprises Ltd., Lantern Science Shenzhen Co. Ltd. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Medicinal Ingredient
Ethyl Alcohol 62 percent

PURPOSE

Purpose
Antiseptic

INACTIVE INGREDIENT

Non Medicinal
Water (Aqua), Glycerin, Isopropyl Myristate, Propylene Glycol,
Tocopheryl Acetate, Aminomethyl Propanol, Carbomer,
Parfum

INDICATIONS & USAGE

Features
- To decrease bacteria on the skin that could cause disease.
- Recommended for repeated use.
- Use anywhere without water.

DOSAGE & ADMINISTRATION

Directions
- Wet hands thoroughly with product and rub 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.
- Keep out of reach of children. In case of accidental ingestion, seek
  professional assistance or contact a Poison Control Center immediately.

WHEN USING

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.

STORAGE AND HANDLING

Other Information
- Do not store above 105 degrees F.
- May disscolor some fabrics.
- Harmful to wood finishes and plastics.

QUESTIONS

This product was not tested on animals.

Made in China

Used under Lic. and Dist. By:
LANTERN ENTERPRISES LTD.
Bellingham, WA 98225
? 1-888-273-7955
Web: LanternBeauty.com

PRINCIPAL DISPLAY PANEL

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

MELLOW INSTANT HAND SANITIZER ORIGINAL  
ethyl alcohol gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 50154-0040
Route of Administration	TOPICAL

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

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
GLYCERIN (UNII: PDC6A3C0OX)
ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
.ALPHA.-TOCOPHEROL ACETATE, D- (UNII: A7E6112E4N)
2-AMINO-2-METHYL-1-PROPANOL (UNII: LU49E6626Q)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 50154-0040-6	59 mL in 1 BOTTLE
2	NDC: 50154-0040-7	236 mL in 1 BOTTLE

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333	12/30/2009

Labeler - Lantern Enterprises Ltd. (240084249)

Establishment
Name	Address	ID/FEI	Business Operations
Lantern Science Shenzhen Co. Ltd		421222423	manufacture