NDC | 65601-754-04, 65601-754-54, 65601-754-55 |
Set ID | 9d18b802-266d-4524-8937-f0e560014b63 |
Category | HUMAN OTC DRUG LABEL |
Packager | Betco Corporation, Ltd. |
Generic Name | |
Product Class | |
Product Number | |
Application Number | PART333E |
- Winning Hands Foaming Antibacterial
- Winning Hands Foaming Antibacterial
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Winning Hands Foaming Antibacterial
Warnings
- For external use only.
- Avoid contact with eyes.
- Children under the age of 6 should be supervised by an adult when using this product.
- Discontinue use is irritation or redness develops.
- If irritation persists for more than 72 hours, consult a physician.
- KEEP OUT OF REACH OF CHILDREN.
- If swallowed, get medical help or contact a Poison Control Center right away.
- Winning Hands Foaming Antibacterial
-
Winning Hands Foaming Antibacterial
Inactive Ingredients
Water, Potassium Cocoate, Propylene Glycol, Glycerin, Tetrasodium EDTA, Fragrance, Bronopol, Sodium Citrate,
Magnesium Nitrate, Sodium Hydroxyacetate, Ethanol, Aloe Barbadensis Leaf Juice, Trisodium Nitriloacetate,
FD&C Yellow #5, Sodium Hydroxide, Methylchloroisothiazolinone, Magnesium Chloride, Methylisothiazolinone,
FD&C Red #40. - Winning Hands Foaming Antibacterial
- Winning Hands Foaming Antibacterial
- Winning Hands Foaming Antibacterial
- Winning Hands Foaming Antibacterial
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INGREDIENTS AND APPEARANCE
WINNING HANDS FOAMING ANTIBACTERIAL
benzalkonium chloride soapProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:65601-754 Route of Administration Topical Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE 13 mg in 1.0 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) POTASSIUM COCOATE (UNII: F8U72V8ZXP) PROPYLENE GLYCOL (UNII: 6DC9Q167V3) GLYCERIN (UNII: PDC6A3C0OX) DITETRACYCLINE TETRASODIUM EDETATE (UNII: WX0A0IT7K5) BRONOPOL (UNII: 6PU1E16C9W) SODIUM CITRATE (UNII: 1Q73Q2JULR) MAGNESIUM NITRATE (UNII: 77CBG3UN78) SODIUM GLYCOLATE (UNII: B75E535IMI) ALCOHOL (UNII: 3K9958V90M) ALOE (UNII: V5VD430YW9) TRISODIUM NITRILOTRIACETATE (UNII: E3C8R2M0XD) FD&C YELLOW NO. 5 (UNII: I753WB2F1M) SODIUM HYDROXIDE (UNII: 55X04QC32I) METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN) MAGNESIUM CHLORIDE (UNII: 02F3473H9O) METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA) FD&C RED NO. 40 (UNII: WZB9127XOA) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:65601-754-54 1000 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 11/12/2012 2 NDC:65601-754-55 208000 mL in 1 DRUM; Type 0: Not a Combination Product 11/12/2012 3 NDC:65601-754-04 3780 mL in 1 JUG; Type 0: Not a Combination Product 11/12/2012 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part333E 11/12/2012 Labeler - Betco Corporation, Ltd. (024492831) Registrant - Betco corporation, Ltd. (024492831) Establishment Name Address ID/FEI Business Operations Betco Corpo, Ltd. 024492831 manufacture(65601-754) , pack(65601-754) , label(65601-754)