Label: FIRST AID ONLY STING RELIEF- benzocaine swab
- NDC Code(s): 0924-5250-01
- Packager: Acme United Corporation
- This is a repackaged label.
- Source NDC Code(s): 46414-2040
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: unapproved drug other
DISCLAIMER: This drug has not been found by FDA to be safe and effective, and this labeling has not been approved by FDA. For further information about unapproved drugs, click here.
Drug Label Information
Updated April 10, 2018
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- Official Label (Printer Friendly)
- ACTIVE INGREDIENT
- PURPOSE
- INDICATIONS & USAGE
- WARNINGS
- KEEP OUT OF REACH OF CHILDREN
-
DOSAGE & ADMINISTRATION
Directions If stinger is present, remove carefully if possible.
Adults Reverse cardboard sleeve so swab is visible. With cardboard sleeve on ampile, crush at dot on sleeve.
There will be a "pop" and the swab will become saturated. Apply saturated applicator to the affected area no more than
3 to 4 times daily.
Children under 2 Consult a doctor.
- INFORMATION FOR PATIENTS
- INACTIVE INGREDIENT
- QUESTIONS
- PRINCIPAL DISPLAY PANEL
-
INGREDIENTS AND APPEARANCE
FIRST AID ONLY STING RELIEF
benzocaine swabProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:0924-5250(NDC:46414-2040) Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength BENZOCAINE (UNII: U3RSY48JW5) (BENZOCAINE - UNII:U3RSY48JW5) BENZOCAINE 0.12 g in 0.6 mL MENTHOL (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A) MENTHOL 0.006 g in 0.6 mL Inactive Ingredients Ingredient Name Strength ISOPROPYL ALCOHOL (UNII: ND2M416302) WATER (UNII: 059QF0KO0R) D&C GREEN NO. 5 (UNII: 8J6RDU8L9X) D&C YELLOW NO. 10 (UNII: 35SW5USQ3G) FD&C BLUE NO. 1 (UNII: H3R47K3TBD) POLYETHYLENE GLYCOL 300 (UNII: 5655G9Y8AQ) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0924-5250-01 10 in 1 CARTON 02/01/2010 1 6 mL in 1 AMPULE; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 02/01/2010 Labeler - Acme United Corporation (001180207) Registrant - Acme United Corporation (001180207) Establishment Name Address ID/FEI Business Operations Acme United Corporation 045924339 relabel(0924-5250) , repack(0924-5250) Establishment Name Address ID/FEI Business Operations Acme United Corporation 080119599 relabel(0924-5250) , repack(0924-5250)