STINGEZE MAX INSECT BITE RELIEF- benzocaine, camphor, phenol liquid 
Wisconsin Pharmacal Company

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

Drug Facts

Active Ingredients

Benzocaine 10%

Phenol 1.35%

Camphor 3%

Purpose

Analgesic, Anesthetic, Antipuritic

First Aid Antiseptic

External Analgesic

Uses

First aid to help prevent infection in minor cuts, scrapes, and burns.

Warnings

For external use only.

When using this product

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

Stop use and ask doctor if

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

Inactive Ingredients

Camphor, Menthyl lactate, Propylene Glycol, SD Alcohol 40B 20%, Water

Questions or Comments?

1-800-558-6614

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STINGEZE  MAX INSECT BITE RELIEF
benzocaine, camphor, phenol liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:68093-7151
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
Benzocaine (UNII: U3RSY48JW5) (Benzocaine - UNII:U3RSY48JW5) Benzocaine0.10 g  in 1 g
Phenol (UNII: 339NCG44TV) (Phenol - UNII:339NCG44TV) Phenol0.0135 g  in 1 g
CAMPHOR (SYNTHETIC) (UNII: 5TJD82A1ET) (CAMPHOR (SYNTHETIC) - UNII:5TJD82A1ET) CAMPHOR (SYNTHETIC)0.03 g  in 1 g
Inactive Ingredients
Ingredient NameStrength
Propylene Glycol (UNII: 6DC9Q167V3)  
Menthyl Lactate, (-)- (UNII: 2BF9E65L7I)  
Alcohol (UNII: 3K9958V90M)  
Water (UNII: 059QF0KO0R)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:68093-7151-11 in 1 CARTON
114.8 g in 1 BOTTLE, WITH APPLICATOR
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart34802/01/2009
Labeler - Wisconsin Pharmacal Company (800873986)
Establishment
NameAddressID/FEIBusiness Operations
Wisconsin Pharmacal Company800873986manufacture(68093-7151)

Revised: 12/2013
Document Id: 8354a619-f4ca-4a16-b040-352c7e47c0ed
Set id: 6ca177d8-e0c3-4582-b45b-ff5ea7879e65
Version: 2
Effective Time: 20131223
 
Wisconsin Pharmacal Company