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Indulgence/propower - Medication Information

Product NDC Code 61307-213
Drug Name

Indulgence/propower

Type Brand
Active Ingredients
Benzalkonium chloride 2.5 mg/l
Route TOPICAL
Dosage Form SOAP
RxCUI drug identifier 1046593
Application Number part333E
Labeler Name U S Chemical Corporation
Packages
Package NDC Code Description
61307-213-10 1 l in 1 bag (61307-213-10)
61307-213-41 1 l in 1 bag (61307-213-41)
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Active ingredient

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

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.
To decrease bacteria on skin, apply small amount, covering hands with product for 30 seconds. Add water, lather, rinse.

Inactive ingredient

A list of inactive, non-medicinal ingredients in a drug product.
Water, cocamidopropyl betaine, cocamidopropyl PG-dimonium chloride phosphate, PEG-6 cocamide, laurtrimonium chloride, aloe barbadensis leaf juice, tocopheryl acetate (vitamin E), fragrance, iodopropynyl butylcarbamate, methylisothiazolinone, yellow 5, red 33.

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.
For handwashing to decrease bacteria on skin.

Purpose

Information about the drug product’s indications for use.
Antibacterial Agent

Spl product data elements

Usually a list of ingredients in a drug product.
Indulgence/ProPower Benzalkonium Chloride COCAMIDOPROPYL PG-DIMONIUM CHLORIDE PHOSPHATE PEG-6 COCAMIDE .ALPHA.-TOCOPHEROL ACETATE IODOPROPYNYL BUTYLCARBAMATE METHYLISOTHIAZOLINONE COCAMIDOPROPYL BETAINE LAURTRIMONIUM CHLORIDE ALOE VERA LEAF WATER FD&C YELLOW NO. 5 D&C RED NO. 33 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.
image image

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. ​EMERGENCY TELEPHONE: 1-866-923-4913

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. Avoid contact with eyes. In case of contact, flush with plenty of water. Stop use and ask a doctor if irritation or rash appears and persists.

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