Label: STING RELIEF PAD- ethyl alcohol, lidocaine swab
NOX-A-STING- ethyl alcohol, lidocaine swab
- NDC Code(s): 0498-0733-00, 0498-0733-10, 0498-0733-34, 0498-1733-34
- Packager: Honeywell Safety Products USA, Inc
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: unapproved drug other
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Drug Label Information
Updated January 19, 2024
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- Sting Relief label
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INGREDIENTS AND APPEARANCE
STING RELIEF PAD
ethyl alcohol, lidocaine swabProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:0498-0733 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength LIDOCAINE HYDROCHLORIDE (UNII: V13007Z41A) (LIDOCAINE - UNII:98PI200987) LIDOCAINE HYDROCHLORIDE ANHYDROUS 20 mg in 1 mL ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL 0.5 mL in 1 mL Inactive Ingredients Ingredient Name Strength BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) MENTHOL (UNII: L7T10EIP3A) WATER (UNII: 059QF0KO0R) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0498-0733-00 0.4 mL in 1 POUCH; Type 0: Not a Combination Product 12/23/2017 2 NDC:0498-0733-34 10 in 1 BOX 12/23/2017 2 0.4 mL in 1 POUCH; Type 0: Not a Combination Product 3 NDC:0498-0733-10 100 in 1 BOX 12/23/2017 3 NDC:0498-0733-00 0.4 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 unapproved drug other 12/23/2017 NOX-A-STING
ethyl alcohol, lidocaine swabProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:0498-1733 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength LIDOCAINE HYDROCHLORIDE (UNII: V13007Z41A) (LIDOCAINE - UNII:98PI200987) LIDOCAINE HYDROCHLORIDE ANHYDROUS 20 mg in 1 mL ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL 0.5 mL in 1 mL Inactive Ingredients Ingredient Name Strength BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) MENTHOL (UNII: L7T10EIP3A) WATER (UNII: 059QF0KO0R) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0498-1733-34 10 in 1 BOX 12/23/2017 1 0.4 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 unapproved drug other 12/23/2017 Labeler - Honeywell Safety Products USA, Inc (118768815) Registrant - Honeywell Safety Products USA, Inc (118768815) Establishment Name Address ID/FEI Business Operations Safetec of America, Inc. 874965262 manufacture(0498-0733, 0498-1733)
