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| Product NDC Code | 76635-001 | ||||||||||||||||||||||||||
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| Drug Name | Antibacterial wipes |
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| Type | Brand | ||||||||||||||||||||||||||
| Active Ingredients |
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| Route | TOPICAL | ||||||||||||||||||||||||||
| Dosage Form | CLOTH | ||||||||||||||||||||||||||
| RxCUI drug identifier | 2360919 | ||||||||||||||||||||||||||
| Application Number | 505G(a)(3) | ||||||||||||||||||||||||||
| Labeler Name | Hangzhou Glamcos Biotech 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) Benzalkonium Chloride 0.2%
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 Peel back flap on front to pull out a towelette. Reseal the flap. No need ro rinse.
Inactive ingredient
A list of inactive, non-medicinal ingredients in a drug product.Inactive ingredients Water，Glycerin，Propylene Glycol，Polyaminopropyl Biguanide，Phenoxyethanol ，Iodopropynyl Butylcarbamate，Green Tea Extract.
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 Kills 99.99% of germs.
Purpose
Information about the drug product’s indications for use.Purpose Antimicrobial
Spl product data elements
Usually a list of ingredients in a drug product.Antibacterial Wipes Benzalkonium Chloride POLYAMINOPROPYL BIGUANIDE GLYCERIN PROPYLENE GLYCOL WATER BENZALKONIUM CHLORIDE BENZALKONIUM GREEN TEA LEAF PHENOXYETHANOL IODOPROPYNYL BUTYLCARBAMATE
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.100 Package Label - Principal Display Panel 100 label front 100 label back
80 Package Label - Principal Display Panel 80 label front 80 label back
40 Package Label - Principal Display Panel label-40 front label-40 back
20 Package Label - Principal Display Panel 20 label front 20 label back
10 Package Label - Principal Display Panel 10 label
400 Pail Label - Principal Display Panel NDC:76635-001-06 NDC:76635-001-07 NDC:76635-001-09 400 label label-400-2 label-400-3
1 Package Label - Principal Display Panel label-1 wipe1 label-1 wipe2
70 Package Label - Principal Display Panel label-70-1 label-70-2
250 Pail Package Label - Principal Display Panel NDC:76635-001-11 label 250 in 1 pail-1 label 250 in 1 pail-2
100 Pail Package Label - Principal Display Panel NDC:76635-001-12 label 100 in 1 pail-1 label 100 in 1 pail-2 label 100 in 1 pail-3
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.
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. Keep out of eyes. In case of eye contact, rinse eyes with water. Stop use and ask a doctor if redness or irritation develops. Keep out of sunlight.
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