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| Product NDC Code | 71734-117 | ||||
|---|---|---|---|---|---|
| Drug Name | Callington anti-bacterial hand sanitizer wipe |
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| Type | Brand | ||||
| Active Ingredients |
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| Route | TOPICAL | ||||
| Dosage Form | SWAB | ||||
| RxCUI drug identifier | 2553300 | ||||
| Application Number | M003 | ||||
| Labeler Name | JIANGMEN SHUIZIRUN SANITARY ARTICLES CO., LTD. | ||||
| Packages |
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Active ingredient
A list of the active, medicinal ingredients in the drug product.Active Ingredient Benzalkonium Chloride .......... 0.05 %
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 Adults and children over 2 years: Tear open packet, unfold and use as a wash cloth. Allow hands to dry without wiping.
Inactive ingredient
A list of inactive, non-medicinal ingredients in a drug product.Inactive Ingredients: Water, Propylene glycol, Polysorbate 20, Dipropylene glycol, Ethylhexyl_x0002_glycerin, Chlorphenesin, Bronopol, 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.Uses: For personal hand hygiene to help prevent the spread of bacteria.
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.Callington Anti-Bacterial Hand Sanitizer Wipe benzalkonium chloride WATER PROPYLENE GLYCOL POLYSORBATE 20 DIPROPYLENE GLYCOL CHLORPHENESIN BRONOPOL BENZALKONIUM CHLORIDE BENZALKONIUM
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.Principal Display Panel
Spl unclassified section
Information not classified as belonging to one of the other fields. Approximately 40% of labeling with effective_time between June 2009 and August 2014 have information in this field.DRUG FACTS
Do not use
Information about all contraindications for use. These contraindications are absolute and are intended for situations in which consumers should not use the product unless a prior diagnosis has been established by a doctor or for situations in which certain consumers should not use the product under any circumstances regardless of whether a doctor or health professional is consulted.For external use only. Do not use in eyes. If this occurs, rinse thoroughly with water. Stop use and ask a doctor if irritation or redness develops and persists for more than 72 hours.
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. Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.
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. If this occurs, rinse thoroughly with water. Stop use and ask a doctor if irritation or redness develops and persists for more than 72 hours. Keep out of reach of children. Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.
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