HEALTHY HANDS SANITIZING HAND WIPES WITH ALOE- benzalkonium chloride cloth
NCH Corporation

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

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Drug Facts

Active ingredient

Benzalkonium chloride 0.13% w/w

Purpose

Antimicrobial

Keep out of reach of children

In case of accidental ingestion, seek medical attention or contact a poison control center immediately.

Uses

 to sanitize hands without requiring water or a rinse
 kills 99.9% of most common germs

Warnings
For external use only

When using this product

 do not use in or near eyes

 discontinue use if irritation and redness develop

Directions

 wet hands thoroughly with wipe  allow to dry without rinsing

Other information

 store at room temperature

Inactive ingredients:

Water, 2-Phenoxyethanol, Alkylpolyglucoside, C 8-10,C10-16, Lauramine, N,N-dimethyl, N-oxide, Tocopherol acetate, Aloe barbadensis leaf juice, PEG-40 Lanolin, Tetrasodium EDTA, Methylchloroisothiazolinone, Methylisothiazolinone.

PRINCIPAL DISPLAY PANEL - 80 Cloth Canister Label

HEALTHY HANDS™
SANITIZING HAND WIPES
with Aloe

Read the entire label before using this product.
• Kills 99.9% of common germs
• Contains Aloe and Vitamin E
• Moisturizes and conditions skin
• Fragrance free
• Fine textured, non-linting Wipe

KEEP OUT OF REACH OF CHILDREN
WARNING
For external use only.

NET CONTENTS: 80 – 6” x 8” Pre-Moistened Wipes

image description

HEALTHY HANDS SANITIZING HAND WIPES WITH ALOE
benzalkonium chloride cloth

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:55533-682
Route of Administration	TOPICAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y)	BENZALKONIUM CHLORIDE	0.0067275 g

Ingredient Name	Strength
Inactive Ingredients
WATER (UNII: 059QF0KO0R)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
DECYL GLUCOSIDE (UNII: Z17H97EA6Y)
LAURAMINE OXIDE (UNII: 4F6FC4MI8W)
ALPHA-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
EDETATE SODIUM (UNII: MP1J8420LU)
METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN)
METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)

#	Item Code	Package Description	Marketing Start Date	Marketing End Date
Packaging
1	NDC:55533-682-97	80 in 1 CANISTER; Type 0: Not a Combination Product	04/29/2014

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC monograph not final	part333E	04/29/2014

Labeler - NCH Corporation (126655562)

Drug Facts Active ingredient