Label: RUSHING FAHS- chloroxylenol solution
- NDC Code(s): 63146-308-10
- Packager: Kay Chemical Company
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated August 20, 2024
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- Active ingredient
- Purpose
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INACTIVE INGREDIENT
Inactive ingredients: water (aqua), potassium cocoate, hexylene glycol, sodium sulfate, tetrasodium EDTA, sodium lauryl sulfate, glycerin, citric acid, coco-glucoside, glyceryl oleate, fragrance, methychloroisothiazolinone, CI 19140 (FD&C Yellow No. 5), methylisothiazolinone, CI 14700 (FDC Red No. 4)
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Principal display panel and representative label
Rushing
1110840
Foaming Antibacterial Hand Soap
Foaming Antibacterial Hand Soap is a rich lather hand soap with
a balanced blend of cleaning agents and skin protecting moisturizers.
KEEP OUT OF REACH OF CHILDREN • FOR INSTITUTIONAL USE ONLY
Chloroxylenol 0.5%
To obtain Spanish Instructions, see outer carton.
Net contents: 42 US fl oz (1250 ml) NDC 63146-308-10
Distributed by | Distribuido por:
SSDC · 4050 Corporate Dr., #100
Grapevine, Texas 76051-2326 USA
Customer Service: (800) 654-8030
©2018 | All rights reserved | Todas los derechos reservados
Made in USA | Hecho en Estados Unidos
774260-00 · RSHGUSA 774260/8000/0918
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INGREDIENTS AND APPEARANCE
RUSHING FAHS
chloroxylenol solutionProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:63146-308 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength CHLOROXYLENOL (UNII: 0F32U78V2Q) (CHLOROXYLENOL - UNII:0F32U78V2Q) CHLOROXYLENOL 5 mg in 1 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) POTASSIUM COCOATE (UNII: F8U72V8ZXP) HEXYLENE GLYCOL (UNII: KEH0A3F75J) SODIUM SULFATE (UNII: 0YPR65R21J) EDETATE SODIUM (UNII: MP1J8420LU) SODIUM LAURYL SULFATE (UNII: 368GB5141J) GLYCERIN (UNII: PDC6A3C0OX) ANHYDROUS CITRIC ACID (UNII: XF417D3PSL) COCO-GLUCOSIDE (UNII: ICS790225B) GLYCERYL OLEATE (UNII: 4PC054V79P) METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN) FD&C YELLOW NO. 5 (UNII: I753WB2F1M) METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA) FD&C RED NO. 4 (UNII: X3W0AM1JLX) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:63146-308-10 1250 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 01/09/2019 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug 505G(a)(3) 01/09/2019 Labeler - Kay Chemical Company (003237021)