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Black ops ab antibacterial foaming - Medication Information

Product NDC Code 79016-103
Drug Name

Black ops ab antibacterial foaming

Type Brand
Active Ingredients
Benzalkonium chloride .13 g/100ml
Route TOPICAL
Dosage Form SOAP
RxCUI drug identifier 1046593
Application Number part333A
Labeler Name Archer Manufacturing, Inc.
Packages
Package NDC Code Description
79016-103-12 1000 ml in 1 pouch (79016-103-12)
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Active ingredient

A list of the active, medicinal ingredients in the drug product.
ACTIVE INGREDIENTS 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. - Pump a small amount of foam into palm of hand. Rub thoroughly over all surfaces of both hands for 15 seconds. Rinse with potable water.

Inactive ingredient

A list of inactive, non-medicinal ingredients in a drug product.
INACTIVE INGREDIENTS Glycerine, PEG/PPG-18/18 Dimethicone, Water

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 FOR HAND WASHING TO HELP REDUCE 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.
BLACK OPS AB ANTIBACTERIAL FOAMING BENZALKONIUM CHLORIDE GLYCERIN WATER PEG/PPG-18/18 DIMETHICONE 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.
01b LBL_Black OPS AB-Dec 21

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 EXPOSED CARTRIDGE OUT OF REACH OF CHILDREN. IF SWALLOWED, GET MEDICAL HELP OR CONTACT POISON CONTROL 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.
WARNINGS FOR EXTERNAL USE ONLY. WHEN USING THIS PRODUCT AVOID CONTACT WITH EYES. IN CASE OF EYE CONTACT, FLUSH WITH WATER. STOP USE AND ASK A DOCTOR IF IRRITATION OR REDNESS DEVELOPS, OR IF CONDITION PERSISTS FOR MORE THAN 72 HOURS.

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