MELLOW INSTANT HAND SANITIZER WITH ALOE AND VITAMIN E- ethyl alcohol gel

Mellow Instant Hand Sanitizer With Aloe and Vitamin E by

Drug Labeling and Warnings

Mellow Instant Hand Sanitizer With Aloe and Vitamin E by is a Otc medication manufactured, distributed, or labeled by Lantern Enterprises Ltd.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Medicinal Ingredient

Ethyl Alcohol 62%

Purpose

Antiseptic

Non-Medicinal

Water, Isopropyl Alcohol, Glycerin, Carbomer, Aminomethyl Propanol, Parfum, Propylene Glycol,, Isopropyl Myristate, Aloe Barbadensis Leaf Juice, Tocopheryl Acetate, FD and C Yellow No. 5 (Tartrazine), FD and C Blue No. 1.

Features

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

Directions

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

Warning

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

INGREDIENTS AND APPEARANCE

MELLOW INSTANT HAND SANITIZER WITH ALOE AND VITAMIN E 
ethyl alcohol gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 50154-0030
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)
ISOPROPYL ALCOHOL (UNII: ND2M416302)
GLYCERIN (UNII: PDC6A3C0OX)
AMINOMETHYLPROPANOL (UNII: LU49E6626Q)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
.ALPHA.-TOCOPHEROL ACETATE, D- (UNII: A7E6112E4N)
FD&C YELLOW NO. 5 (UNII: I753WB2F1M)
FD&C BLUE NO. 1 (UNII: H3R47K3TBD)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 50154-0030-4	59 mL in 1 BOTTLE
2	NDC: 50154-0030-5	236 mL in 1 BOTTLE

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	12/30/2009

Labeler - Lantern Enterprises Ltd. (240084249)