ZILACTIN  EARLY RELIEF COLD SORE - benzyl alcohol gel 
Applied Laboratories, Inc.

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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Zilactin Red Applied

Drug Facts

Active ingredient

Benzyl alcohol 10%

Purpose

Cold sore/fever blister treatment, Oral pain reliever

Use

temporarily relieves pain caused by:

Warnings

Flammable:

  • keep away from fire or flame

Stop use and ask a physician if

  • sore mouth symptoms do not improve in 7 days
  • condition worsens or symptoms clear up and occur again within a few days
  • swelling, rash or fever develops
  • irritation, pain or redness persists or worsens
  • apply only to affected area
  • do not exceed recommended dosage
  • avoid contact with the eyes
  • do not use for more than 7 days unless directed by a physician or dentist

Keep out of reach of children. If swallowed, get medical help or contact a poison control center immediately.

Directions

adults and children
2 years and older
dry affected area. Apply with cotton swab or clean finger up to 4 times daily. Allow to dry 30-60 seconds.
children under 12 years adult supervision should be given in the use of this product
children under 2 years do not use, consult a physician or dentist

Other information

Inactive ingredients

boric acid, hydroxypropylcellulose, propylene glycol, purified water, salicylic acid, SD alcohol 37, tannic acid

Manufactured for: Blairex Laboratories, Inc. P.O. Box 2127 Columbus, IN 47202 USA

Telephone
Questions or Comments?
Call TOLL FREE 1-800-252-4739
www.zilactin.com

PROMOTES HEALING

Cold Sore/Fever Blister/Oral Pain Treatment

Zilactin ® Early Relief Cold Sore Gel

Net wt. 0.25 oz (7.1g)

Principal Display Panel
ZILACTIN   EARLY RELIEF COLD SORE
benzyl alcohol gel
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:72751-0301
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
BENZYL ALCOHOL (UNII: LKG8494WBH) (BENZYL ALCOHOL - UNII:LKG8494WBH) BENZYL ALCOHOL0.1 g  in 1 g
Inactive Ingredients
Ingredient NameStrength
BORIC ACID (UNII: R57ZHV85D4)  
HYDROXYPROPYL CELLULOSE (1200000 WAMW) (UNII: U3JF91U133)  
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
SALICYLIC ACID (UNII: O414PZ4LPZ)  
ALCOHOL (UNII: 3K9958V90M)  
EUCALYPTOL (UNII: RV6J6604TK)  
THYMOL (UNII: 3J50XA376E)  
MENTHOL, UNSPECIFIED FORM (UNII: L7T10EIP3A)  
TANNIC ACID (UNII: 28F9E0DJY6)  
WATER (UNII: 059QF0KO0R)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:72751-0301-11 in 1 CARTON06/30/2005
17.1 g in 1 TUBE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart35606/30/2005
Labeler - Applied Laboratories, Inc. (117337220)

Revised: 12/2021
Document Id: d21c275e-697d-e95e-e053-2a95a90ad633
Set id: 402e7786-c53a-4e8d-ba6a-5e56ce74d63e
Version: 4
Effective Time: 20211201
 
Applied Laboratories, Inc.