UNITED AIRLINES CLEAN PLUS CLOROX- ethyl alcohol liquid

United Airlines Clean Plus Clorox by

Drug Labeling and Warnings

United Airlines Clean Plus Clorox by is a Otc medication manufactured, distributed, or labeled by Freshorize LLC, Freshorize USA Ltd.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Uses:

To help decrease bacteria on skin.

Warnings:

Flammable.
Keep away from fire or flame.
For external use only.
Do not use in eyese, in case of contact, rinse eyes thoroughly with water.
Stop use and ask a doctor if skin irritation develops.

Warnings:

Keep out of reach of children.
If swallowed, get medical help or contact a Poison Control Center right away.

Directions:

Place/use enough product to cover hands, rub hands together until dry.
Supervise children in the use of the product.

Drug Facts:

Active Ingredients: Ethyl Alcohol 62% v/v

Inactive Ingredients:

Aloe Barbadensis Leaf Extract
Aqua

Carbomer
Glycerin

Propylene Glycol

Tocopheryl Acetate

Triethanolamine

Other Information:

Avoid extreme temperatures.

Purpose:

Antibacterial

Product Label

Does not contain bleach

Listed on the label: Use enough product to cover the hands

INGREDIENTS AND APPEARANCE

UNITED AIRLINES CLEAN PLUS CLOROX 
ethyl alcohol liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 52305-225
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
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)	0.001 mL  in 100 mL
CARBOMER 934 (UNII: Z135WT9208)	0.28 mL  in 100 mL
ALOE VERA LEAF (UNII: ZY81Z83H0X)	0.001 mL  in 100 mL
WATER (UNII: 059QF0KO0R)	37.307 mL  in 100 mL
TROLAMINE (UNII: 9O3K93S3TK)	0.11 mL  in 100 mL
GLYCERIN (UNII: PDC6A3C0OX)	0.3 mL  in 100 mL
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)	0.001 mL  in 100 mL

Product Characteristics
Color		Score
Shape		Size
Flavor		Imprint Code
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 52305-225-25	250 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product	08/28/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	505G(a)(3)	08/28/2020

Labeler - Freshorize LLC (424168503)

Registrant - Freshorize USA Ltd. (018206924)