BITEMD EXTERNAL ANALGESIC FIRST AID ANTISEPTIC- benzocaine, camphor (synthetic), and phenol liquid 
United Industries 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.

----------

BiteMD® External Analgesic First Aid Antiseptic

DRUG FACTS

Active Ingredients:Purpose:
Benzocaine 5%Analgesic, Anesthetic, Antipruritic
Camphor 3%Topical Analgesic
Phenol 1.35%First Aid Antiseptic

Uses

First aid for temporary relief of:

Warnings

For external use only

When using this product

  • Do not get in eyes.
  • Do not apply over large areas of the body or bandage.
  • In case of deep or puncture wounds, animal bites or serious burns, consult a doctor.

Stop use and ask doctor if condition worsens; or if symptoms persist for more than 7 days, clear up and occur again within a few days. Do not use longer than one week unless directed by doctor.

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away. If in eyes, flush with water for 15 minutes and call a physician.

Directions

Other Information

Adult and children 2 years and over

Apply to affected area 1 to 3 times daily

Children under 2 years

Consult a doctor

Inactive Ingredients

Propylene Glycol

Questions or Comments?

Call 1-800-767-9927.

Manufactured by
Wisconsin Pharmacal Company, LLC
Jackson, WI 53037 USA
Distributed by Spectrum
Division of United Industries Corporation
PO Box 142642, St. Louis, MO 63114-0642

PRINCIPAL DISPLAY PANEL - 14.7 mL Bottle Label

BiteMD®

External Analgesic
First Aid Antiseptic

from the makers of
Cutter®
BRAND

INSECT
BITE RELIEF

STOPS PAIN
RELIEVES ITCHING
REDUCES INFECTION

Chiggers
Wasps
Mosquitoes
Ticks

Soft Tip For
Controlled Application

Net 0.5 fl oz (14.7 mL)

PRINCIPAL DISPLAY PANEL - 14.7 mL Bottle Label
BITEMD EXTERNAL ANALGESIC FIRST AID ANTISEPTIC 
benzocaine, camphor (synthetic), and phenol liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:79364-0932
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
Benzocaine (UNII: U3RSY48JW5) (Benzocaine - UNII:U3RSY48JW5) Benzocaine0.0524 mg  in 1 mL
CAMPHOR (SYNTHETIC) (UNII: 5TJD82A1ET) (CAMPHOR (SYNTHETIC) - UNII:5TJD82A1ET) CAMPHOR (SYNTHETIC)0.03144 mg  in 1 mL
Phenol (UNII: 339NCG44TV) (Phenol - UNII:339NCG44TV) Phenol0.01572 mg  in 1 mL
Inactive Ingredients
Ingredient NameStrength
Propylene Glycol (UNII: 6DC9Q167V3)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:79364-0932-114.7 mL in 1 BOTTLE; Type 0: Not a Combination Product01/01/2020
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart34801/01/2020
Labeler - United Industries Corporation (068527704)
Establishment
NameAddressID/FEIBusiness Operations
Wisconsin Pharmacal800873986MANUFACTURE(79364-0932)

Revised: 1/2023
Document Id: 11b330c8-e9fa-4ae4-a1cd-a63463855e5b
Set id: 4c60db03-6d2b-4ae0-a200-718b3a50eb0f
Version: 2
Effective Time: 20230112
 
United Industries Corporation