Label: STING-KILL- benzocaine and menthol solution
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Contains inactivated NDC Code(s)
NDC Code(s): 52412-250-20, 52412-250-21 - Packager: Randob Ltd.
- 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 February 13, 2017
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- Official Label (Printer Friendly)
- Active ingredients
- Purpose
- Keep Out of Reach of Children
- Uses
- Warnings
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Directions
Children under 2 yrs.
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- Do not use
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- Consult doctor
Adults and children 2 yrs. and older
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- Apply to affected area as needed but not more than 3 to 4 times a day.
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- (1) Bee stings only, remove stinger before treatment.
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- (2) Tear foil pack at notch, exposing pad.
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- (3) Apply immediately to bite or sting area. Dispose of pad after use.
- Inactive Ingredients
- Package/Label Principal Display Panel
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INGREDIENTS AND APPEARANCE
STING-KILL
benzocaine and menthol solutionProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:52412-250 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength BENZOCAINE (UNII: U3RSY48JW5) (BENZOCAINE - UNII:U3RSY48JW5) BENZOCAINE 200 mg in 1 mL MENTHOL (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A) MENTHOL 10 mg in 1 mL Inactive Ingredients Ingredient Name Strength FD&C BLUE NO. 1 (UNII: H3R47K3TBD) ISOPROPYL ALCOHOL (UNII: ND2M416302) PEG-8 LAURATE (UNII: 762O8IWA10) WATER (UNII: 059QF0KO0R) Product Characteristics Color BLUE (Blue) Score Shape Size Flavor Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:52412-250-20 8 in 1 BLISTER PACK 01/01/1965 1 0.56 mL in 1 POUCH; Type 0: Not a Combination Product 2 NDC:52412-250-21 8 in 1 CARTON 01/15/2017 2 0.56 mL in 1 POUCH; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part348 01/01/1965 Labeler - Randob Ltd. (061995007) Registrant - Randob Ltd. (061995007)