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| Product NDC Code | 71734-210 | ||||
|---|---|---|---|---|---|
| Drug Name | Callington anti-bacterial hand sanitiser |
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| Type | Brand | ||||
| Active Ingredients |
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| Route | TOPICAL | ||||
| Dosage Form | CLOTH | ||||
| Application Number | part333A | ||||
| Labeler Name | JIANGMEN SHUIZIRUN SANITARY ARTICLES 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 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 Tear open packedt, unfold and use as 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, Ethylhexylglycerin, 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: Antiseptic cleansing of hands to decrease bacteria on skin without the use of soap and water.
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 Sanitiser BENZALKONIUM CHLORIDE BENZALKONIUM CHLORIDE BENZALKONIUM PROPYLENE GLYCOL POLYSORBATE 20 Water DIPROPYLENE GLYCOL ETHYLHEXYLGLYCERIN CHLORPHENESIN BRONOPOL
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 o 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. 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.For external use only. for external use only. do not use in eyes. If this occurs, rinse thoroughly with water. Stop use and ask a doctor if irritation o redness develops and persists for more than 72 hours. 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