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| Product NDC Code | 79618-001 | ||||||||||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Drug Name | Alcohol wipe |
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| Type | Brand | ||||||||||||||||||
| Active Ingredients |
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| Route | TOPICAL | ||||||||||||||||||
| Dosage Form | CLOTH | ||||||||||||||||||
| RxCUI drug identifier | 1307051 | ||||||||||||||||||
| Application Number | part333A | ||||||||||||||||||
| Labeler Name | YAHON ENTERPRISE CO.,LTD | ||||||||||||||||||
| 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(s) Ethyl Alcohol 75% (alc/vol)
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 Open cap, remove seal and pull wipes out. Discard after single use and do not flush Keep cap and seal tightly closed between uses to prevent from drying out.
Inactive ingredient
A list of inactive, non-medicinal ingredients in a drug product.Inactive ingredients Water, Benzalkonium Chloride, Polyaminopropyl Biguanide, Citric Acid
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 Sanitizing wipes to help reduce bacteria on the skin or surfaces
Purpose
Information about the drug product’s indications for use.Purpose Antiseptic
Spl product data elements
Usually a list of ingredients in a drug product.Alcohol Wipe ALCOHOL BENZALKONIUM CHLORIDE CITRIC ACID ACETATE WATER ALCOHOL ALCOHOL POLYAMINOPROPYL BIGUANIDE
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.Package Label - Principal Display Panel Front Label Bck Label Drug Facts Whole Package
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.Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.
Stop use
Information about when use of the drug product should be discontinued immediately and a doctor consulted. Includes information about any signs of toxicity or other reactions that would necessitate immediately discontinuing use of the product.Stop use and ask a doctor if you have deep or puncture wounds, animal bites serious burns Irritation and redness develop or condition persists for more than 72 hours
When using
Information about side effects that people may experience, and the substances (e.g. alcohol) or activities (e.g. operating machinery, driving a car) to avoid while using the drug product.Avoid contact with eyes. If in eyes, remove contact lenses (if any), rinse slowly with water or get medical help.
Storage and handling
Information about safe storage and handling of the drug product.Other information Do not apply internally. Store in a cool dry place below 30˚C
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 Flammable, keep away from heat, spark, electrical fire or flame.
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