MOUTH SORE MEDICATION- benzocaine liquid 
Zee Medical

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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COMPARE TO THE ACTIVE INGREDIENT IN KANK-A®

ZEE MOUTH SORE MEDICATION

ORAL PAIN RELIEVER

Fast Mouth Sore Relief

25 Packets

0.5g (0.017 oz) per packet

DO NOT USE IF PACKET IS TORN OR OPEN

Drug Facts

Active ingredient

Benzocaine 20% (w/w)

Purpose

Oral pain reliever

Uses

temporarily relieves pain caused by

Warnings

For oral use only. Avoid contact with eyes.

Allergy alert: do not use this product if you have a history of allergy to local anesthetics such as procaine, butacaine, benzocaine, or other “caine” anesthetics

When using this product do not use for more than 7 days unless directed by a dentist or doctor. If sore mouth symptoms do not improve e in 7 days; if irritation, pain or redness persists or worsens; or if swelling, rash or fever develops, see your doctor or dentist promptly. Do not exceed recommended dosage.

Keep out of reach of children. If more than used for pain relief is accidentally swallowed, get medical help or contact a Poison Control Center right away.

Directions

Inactive ingredients

PEG 400, PEG 3350, peppermint oil, sodium saccharin, sorbic acid

Questions?

1-800-841-8417

Distributed by
Zee Medical, Inc., Irvine,CA 92606
This product is not manufactured or distributed by Blistex, Inc., distributor of KANK-A® Mouth Pain Liquid

PRINCIPAL DISPLAY PANEL – packet label

DO NOT USE IF PACKET IS TORN OR OPEN

MOUTH SORE ZEE

MEDICATION

Oral Pain Reliever

Fast Mouth Sore Relief

5g (0.017 oz)

PRINCIPAL DISPLAY PANEL – packet label

PRINCIPAL DISPLAY PANEL – Carton label

NDC 35418-631-01

COMPARE TO THE ACTIVE INGREDIENT IN KANK-A®*

ZEE MOUTH SORE MEDICATION

ORAL PAIN RELIEVER

Fast Mouth Sore Relief

25 Packets

0.5g (0.017 oz) per packet

PRINCIPAL DISPLAY PANEL – Carton label
MOUTH SORE MEDICATION 
benzocaine liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:35418-631
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
benzocaine (UNII: U3RSY48JW5) (benzocaine - UNII:U3RSY48JW5) benzocaine200 mg  in 1 g
Inactive Ingredients
Ingredient NameStrength
polyethylene glycol 400 (UNII: B697894SGQ)  
polyethylene glycol 3350 (UNII: G2M7P15E5P)  
peppermint oil (UNII: AV092KU4JH)  
saccharin sodium dihydrate (UNII: SB8ZUX40TY)  
sorbic acid (UNII: X045WJ989B)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:35418-631-0125 in 1 BOX
10.5 g in 1 PACKET; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart35605/01/2010
Labeler - Zee Medical (009645623)
Registrant - Safetec of America, Inc. (874965262)
Establishment
NameAddressID/FEIBusiness Operations
Safetec Of America, Inc.874965262MANUFACTURE(35418-631)

Revised: 6/2014
Document Id: c54dcee0-8b21-4856-8391-d8ce5b4d0b8e
Set id: 2666b95e-667f-471a-9929-9deca27e9cbc
Version: 2
Effective Time: 20140623
 
Zee Medical