Label: RUSHING FAHS- chloroxylenol solution
- NDC Code(s): 63146-308-10
- Packager: Kay Chemical Co.
- 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 November 14, 2022
If you are a consumer or patient please visit this version.
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- Active ingredient
- Purpose
- Uses
- Warnings
- Directions
- Other Information
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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) CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP) 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 not final part333E 01/09/2019 Labeler - Kay Chemical Co. (003237021)