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| Product NDC Code | 65585-562 | ||||||||||||||||||
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| Drug Name | Whiskcare 362 |
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| Type | Brand | ||||||||||||||||||
| Active Ingredients |
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| Route | TOPICAL | ||||||||||||||||||
| Dosage Form | SOAP | ||||||||||||||||||
| RxCUI drug identifier | 1045003 | ||||||||||||||||||
| Application Number | 505G(a)(3) | ||||||||||||||||||
| Labeler Name | Whisk Products, Inc. | ||||||||||||||||||
| Packages |
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| Check if available Online | Get Medication Prices online with Discount |
Active ingredient
A list of the active, medicinal ingredients in the drug product.Active Ingredient Chloroxylenol 0.75% w/w
Dosage and administration
Information about the drug product’s dosage and administration recommendations, including starting dose, dose range, titration regimens, and any other clinically sigificant information that affects dosing recommendations.Directions Wet hands and forearms. Apply a small amount (5 mL) or palmful to hands and forearms. Scrub thoroughly for at least fifteen seconds. Rinse completely and dry.
Inactive ingredient
A list of inactive, non-medicinal ingredients in a drug product.Inactive Ingredients Water, Sodium Laureth Sulfate, TEA-Lauryl SUlfate, Cocamidopropyl Betaine, Tetrasodium EDTA, Fragrance, Polyquaternium-7, Sodium Chloride, DMDM Hydantoin, Blue 1
Indications and usage
A statement of each of the drug products indications for use, such as for the treatment, prevention, mitigation, cure, or diagnosis of a disease or condition, or of a manifestation of a recognized disease or condition, or for the relief of symptoms associated with a recognized disease or condition. This field may also describe any relevant limitations of use.Use reduces amount of bacteria on hands
Purpose
Information about the drug product’s indications for use.Purpose Skin Antimicrobial
Spl product data elements
Usually a list of ingredients in a drug product.WhiskCare 362 Chloroxylenol DMDM HYDANTOIN CHLOROXYLENOL CHLOROXYLENOL WATER TRIETHANOLAMINE LAURYL SULFATE SODIUM CHLORIDE FD&C BLUE NO. 1 COCAMIDOPROPYL BETAINE SODIUM LAURETH SULFATE EDETATE SODIUM POLYQUATERNIUM-7 (70/30 ACRYLAMIDE/DADMAC; 1600000 MW) aqua blue
Package label principal display panel
The content of the principal display panel of the product package, usually including the product’s name, dosage forms, and other key information about the drug product.Case Label 8 x 1000 mL Bags
Keep out of reach of children
Information pertaining to whether the product should be kept out of the reach of children, and instructions about what to do in the case of accidental contact or ingestion, if appropriate.Not for use on children under 6 months of age. For institutional and professional use only.
Warnings
Information about serious adverse reactions and potential safety hazards, including limitations in use imposed by those hazards and steps that should be taken if they occur.Warnings For external use only. Do not use in eyes. Discontinue use if irritation and redness develop. If condition persists for more than 72 hours, consult a physician. Not for use on children under 6 months of age. For institutional and professional use only.
Disclaimer: Do not rely on openFDA or Phanrmacy Near Me to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. Source: OpenFDA, Healthporta Drugs API