ONID WIPE- ethanol swab
ONID Technology Corp

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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Active Ingredient

Ethyl Alcohol 75%

Purpose

Antiseptic

Uses

For hand washing to decrease bacteria on the skin
Reccomended for repeated use

Directions

open packet
remove and unfold wipe
wipe hands throughly for approximately 15 seconds
do not flush

Keep Out of Reach of Children

If swollowed get medical help or contact Poision Control Center imediately.

Inactive Ingredients

Taiwan Hinoki oil, titanium dioxide, water

Principal Display Panel

image description

ONID WIPE
ethanol swab

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:71441-180
Route of Administration	TOPICAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	75 mL in 100 mL

Ingredient Name	Strength
Inactive Ingredients
Water (UNII: 059QF0KO0R)	24.9 mL in 100 mL
TITANIUM DIOXIDE (UNII: 15FIX9V2JP)	1 mL in 100 mL
CHAMAECYPARIS OBTUSA WOOD OIL (UNII: P2OMP71Y62)	.1 mL in 100 mL

Product Characteristics
Color	white	Score
Shape	RECTANGLE	Size
Flavor		Imprint Code
Contains

#	Item Code	Package Description	Marketing Start Date	Marketing End Date
Packaging
1	NDC:71441-180-10	.82 mL in 1 PACKET; Type 0: Not a Combination Product	06/28/2017

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC monograph not final	part333E	06/28/2017

Labeler - ONID Technology Corp (658461764)

Registrant - ONID Technology Corp (658461764)

Name	Address	ID/FEI	Business Operations
Establishment
Diamond Wipes International		161104729	manufacture(71441-180)