TRUE WASH INSTANT HAND SANITIZER- alcohol gel

True Wash Instant Hand Sanitizer by

Drug Labeling and Warnings

True Wash Instant Hand Sanitizer by is a Otc medication manufactured, distributed, or labeled by Supply Chain Sources LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Drug Facts

Active ingredient

Ethyl Alcohol 75%

Purpose

Antiseptic

Uses

• For hand sanitizing to decrease bacteria on the skin
• Recommended for repeated use

Warnings

For external use only

When using this product:

avoid contact with eyes.  In case of eye contact, flush eyes with water.

Stop use and ask a doctor if:

irritation or redness develops, of if condition persists for more than 72 hours.

Keep out of reach of children.

If swallowed, get medical help or contact a Poison Control Center right away.

Directions:

Squeeze appropriate amount of sanitizer on to hands and rub together until dry.  Use as needed.  For children under 6, use with adult supervision.  Not recommended for infants.

Inactive ingredients:

Water, Aloe Barbadensis Leaf Extract, Acrylates/C10-30 alkyl Acrylate Crosspolymer, Tetrahydroxypropyl Ethylenediamine

Package Labeling: 250 mL (

75478-007-00)

Package Labeling: 500 mL (

75478-007-01)

Package Labeling: 60 mL (

75478-007-02)

INGREDIENTS AND APPEARANCE

TRUE WASH INSTANT HAND SANITIZER 
alcohol gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 75478-007
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	0.75 mL  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
CARBOMER INTERPOLYMER TYPE A (ALLYL SUCROSE CROSSLINKED) (UNII: 59TL3WG5CO)
EDETOL (UNII: Q4R969U9FR)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 75478-007-00	250 mL in 1 BOTTLE; Type 0: Not a Combination Product	05/20/2020
2	NDC: 75478-007-01	500 mL in 1 BOTTLE; Type 0: Not a Combination Product	05/20/2020
3	NDC: 75478-007-02	60 mL in 1 BOTTLE; Type 0: Not a Combination Product	05/20/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333E	05/20/2020

Labeler - Supply Chain Sources LLC (080660498)

Establishment
Name	Address	ID/FEI	Business Operations
GUANGZHOU ORCHARD AROMATHERAPY & SKIN CARE CO.,LTD		542355899	manufacture(75478-007) , label(75478-007)