Label: STINGEZE MAX INSECT BITE RELIEF- benzocaine, camphor, phenol liquid
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Contains inactivated NDC Code(s)
NDC Code(s): 68093-7151-1 - Packager: Wisconsin Pharmacal Company
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: OTC monograph not final
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.
Drug Label Information
Updated December 23, 2013
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- Official Label (Printer Friendly)
- Drug Facts
- Uses
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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.
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Directions
- Clean area
- Apply a small amount to the bite area while massaging with sponge tip applicator. If itching persists, apply again in 10-15 minutes
- For ticks and bees, remove tick or stinger before treatment
- Adults and children 2 years and over: Apply to affected area 1 to 3 times daily
- Children under 2 years: Consult a doctor
- Inactive Ingredients
- Questions or Comments?
- PRINCIPAL DISPLAY PANEL
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
STINGEZE MAX INSECT BITE RELIEF
benzocaine, camphor, phenol liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:68093-7151 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength Benzocaine (UNII: U3RSY48JW5) (Benzocaine - UNII:U3RSY48JW5) Benzocaine 0.10 g in 1 g Phenol (UNII: 339NCG44TV) (Phenol - UNII:339NCG44TV) Phenol 0.0135 g in 1 g CAMPHOR (SYNTHETIC) (UNII: 5TJD82A1ET) (CAMPHOR (SYNTHETIC) - UNII:5TJD82A1ET) CAMPHOR (SYNTHETIC) 0.03 g in 1 g Inactive Ingredients Ingredient Name Strength Propylene Glycol (UNII: 6DC9Q167V3) Menthyl Lactate, (-)- (UNII: 2BF9E65L7I) Alcohol (UNII: 3K9958V90M) Water (UNII: 059QF0KO0R) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:68093-7151-1 1 in 1 CARTON 1 14.8 g in 1 BOTTLE, WITH APPLICATOR Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part348 02/01/2009 Labeler - Wisconsin Pharmacal Company (800873986) Establishment Name Address ID/FEI Business Operations Wisconsin Pharmacal Company 800873986 manufacture(68093-7151)