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| Product NDC Code | 76906-002 | ||||||||||||||||||||||||||||||||||||
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| Drug Name | Wet wipe |
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| Type | Brand | ||||||||||||||||||||||||||||||||||||
| Active Ingredients |
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| Route | TOPICAL | ||||||||||||||||||||||||||||||||||||
| Dosage Form | SWAB | ||||||||||||||||||||||||||||||||||||
| RxCUI drug identifier | 1038558 | ||||||||||||||||||||||||||||||||||||
| Application Number | part333A | ||||||||||||||||||||||||||||||||||||
| Labeler Name | Zhejiang BeiTao Hygienic Products 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 0.13% Purpose Antimicrobial
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 For hand sanitizing to decrease bacteria on the skin. Recommended for repeated use.
Inactive ingredient
A list of inactive, non-medicinal ingredients in a drug product.Inactive ingredients Aqua, Propylene Glycol, Polysorbate 20, Phenoxyethanol.
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 For hand washing to decrease bacteria on the skin. Recommended for repeated use.
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.Wet Wipe BENZALKONIUM CHLORIDE WATER POLYSORBATE 20 PROPYLENE GLYCOL PHENOXYETHANOL 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.80 POUCH in 1 BAG NDC: 76906-002-06 20 POUCH in 1 BAG NDC: 76906-002-02 80PCS NDC 76906-002-13 10PCS NDC 76906-002-16 80PCS NDC 76906-002-17 40 PCS NDC 76906-002-15 80 PCS NDC 76906-002-14 1 80 pouch 20 wet 002 80PCS 0.13 10 PCS 80 PCS 15 14
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.Warning For external use only When using this product, avoid contact with the eyes. In case of contact, flush eyes thoroughly with water. Stop use and ask a doctor if irritation and redness develop. 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