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Zep acclaim ab - Medication Information

Product NDC Code 66949-131
Drug Name

Zep acclaim ab

Type Brand
Active Ingredients
Benzalkonium chloride .13 g/100ml
Route TOPICAL
Dosage Form LIQUID
RxCUI drug identifier 1046593
Application Number 505G(a)(3)
Labeler Name Zep Inc.
Packages
Package NDC Code Description
66949-131-01 11400 ml in 1 case (66949-131-01)
66949-131-11 6000 ml in 1 case (66949-131-11)
66949-131-16 6000 ml in 1 case (66949-131-16)
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Active ingredient

A list of the active, medicinal ingredients in the drug product.
Active Ingredient Benzalkonium Chloride 0.13%

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 Wet hands with water. Place hands under dispenser and apply liquid soap. Massage soap into hands and wrists, emphasizing back of hands, knuckles, and cuticles.

Inactive ingredient

A list of inactive, non-medicinal ingredients in a drug product.
Inactive Ingredients Water, Cetrimonium Chloride, Lauryl/Myristyl Amidopropyl Amine Oxide, Glycerin, Cocamide DIPA, PEG-120 Methyl Glucose Dioleate, Sodium Chloride, Citric Acid, Methylchloroisothiazolinone, Methylisothiazolinone, Tetrasodium EDTA, Fragrance, Yellow 5, Red 4

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 Hand washing to decrease bacteria on skin.

Purpose

Information about the drug product’s indications for use.
Purpose Antiseptic Hand Wash

Spl product data elements

Usually a list of ingredients in a drug product.
Zep Acclaim AB Benzalkonium Chloride BENZALKONIUM CHLORIDE BENZALKONIUM WATER GLYCERIN FD&C YELLOW NO. 5 SODIUM CHLORIDE ANHYDROUS CITRIC ACID LAUROYL/MYRISTOYL AMIDOPROPYL AMINE OXIDE COCO DIISOPROPANOLAMIDE PEG-120 METHYL GLUCOSE DIOLEATE METHYLCHLOROISOTHIAZOLINONE EDETATE SODIUM EDETIC ACID FD&C RED NO. 4 CETRIMONIUM CHLORIDE METHYLISOTHIAZOLINONE

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.
131_3149

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.
Do not use Do not use in the eyes; if in eyes, rinse promptly and thoroughly with water.

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 except under adult supervision.

Other safety information

Information about safe use and handling of the product that may not have been specified in another field.
Other Information Store at room temperature. Do not freeze. Dispose in accordance with all applicable federal, state, and local regulations.

Questions

A telephone number of a source to answer questions about a drug product. Sometimes available days and times are also noted.
Questions or comments? Call 1-877-BUY-ZEP (1-877-428-9937)

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 Stop use and ask a doctor if skin irritation or redness 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.
When using this product Do not swallow. If swallowed, do not induce vomiting and if individual is conscious, give large quantities of water to drink and consult a physician immediately.

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.

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