DREAMY GLOW HAND SANITIZER 01- alcohol liquid

Dreamy Glow hand sanitizer by

Drug Labeling and Warnings

Dreamy Glow hand sanitizer by is a Otc medication manufactured, distributed, or labeled by Shenzhen Lantern Cosmetic Co Ltd, Townley Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Drug Facts

Medicical Ingredient

Medicical Ingredient Purpose

Ethyl Alcohol 65% Antiseptic

Features

To decrease bacteria on the skin that could cause disease.

Recommended for repeated use.

use anywhere without water.

Warning

For external use only.

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 poson control center immediately.

Non-Medicinal

Water, Fragrance, carbomer, CI 42090, CI15985

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.

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 105F.

May discolor some fabrics.

Harmful to wood finishes and plastics.

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

DREAMY GLOW HAND SANITIZER  01
alcohol liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 54860-132
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	65 mL  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
CARBOMER 940 (UNII: 4Q93RCW27E)	0.26 mL  in 100 mL
WATER (UNII: 059QF0KO0R)	34.2597 mL  in 100 mL
PEACH (UNII: 3OKE88I3QG)	0.4 mL  in 100 mL
FD&C RED NO. 4 (UNII: X3W0AM1JLX)	0.00002 mL  in 100 mL
AMINOMETHYLPROPANOL (UNII: LU49E6626Q)	0.08 mL  in 100 mL
FD&C YELLOW NO. 6 (UNII: H77VEI93A8)	0.00028 mL  in 100 mL

Product Characteristics
Color	orange	Score
Shape		Size
Flavor		Imprint Code
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 54860-132-01	29 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	11/05/2019

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	11/05/2019

Labeler - Shenzhen Lantern Cosmetic Co Ltd (421222423)

Registrant - Townley Inc. (016956158)

Establishment
Name	Address	ID/FEI	Business Operations
Shenzhen Lantern Cosmetic Co Ltd		421222423	manufacture(54860-132)