NDC 11822-1234 Anorectal

NDC Product Code 11822-1234

NDC 11822-1234-1

Package Description: 1 TUBE in 1 CARTON > 28.3 mL in 1 TUBE

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.

NDC Product Information

Anorectal with NDC 11822-1234 is a product labeled by Rite Aid. The generic name of Anorectal is . The product's dosage form is and is administered via form.

Labeler Name: Rite Aid

Dosage Form: -

Product Type: What kind of product is this?
Indicates the type of product, such as Human Prescription Drug or Human Over the Counter Drug. This data element matches the “Document Type” field of the Structured Product Listing.

Inactive Ingredient(s)

About the Inactive Ingredient(s)
The inactive ingredients are all the component of a medicinal product OTHER than the active ingredient(s). The acronym "UNII" stands for “Unique Ingredient Identifier” and is used to identify each inactive ingredient present in a product.

  • WATER (UNII: 059QF0KO0R)

Product Labeler Information

What is the Labeler Name?
Name of Company corresponding to the labeler code segment of the Product NDC.

Labeler Name: Rite Aid
Labeler Code: 11822
Start Marketing Date: 03-24-2016 What is the Start Marketing Date?
This is the date that the labeler indicates was the start of its marketing of the drug product.

Listing Expiration Date: 12-31-2019 What is the Listing Expiration Date?
This is the date when the listing record will expire if not updated or certified by the product labeler.

Exclude Flag: I What is the NDC Exclude Flag?
This field indicates whether the product has been removed/excluded from the NDC Directory for failure to respond to FDA’s requests for correction to deficient or non-compliant submissions. Values = ‘Y’ or ‘N’.

* Please review the disclaimer below.

Anorectal Product Label Images

Anorectal Product Labeling Information

The product labeling information includes all published material associated to a drug. Product labeling documents include information like generic names, active ingredients, ingredient strength dosage, routes of administration, appearance, usage, warnings, inactive ingredients, etc.

Product Labeling Index

Active Ingredient                               Purpose

Lidocaine 5%......................................Local anesthetic

Warningsfor External Use Only

When using this product do not get into eyes.Stop use and ask a doctor if • condition worsens or doesnot improve within 7 days • do not exceed therecommended daily dosage unless directed by a doctor• in case of bleeding, consult a doctor promptly • do notput this product into the rectum by using fingers or anymechanical device or applicatorCertain persons can develop allergic reactions to ingredients in thisproduct. If the symptom being treated does not subside or if redness, irritation, swelling, pain, or other symptoms develop orincrease, discontinue use and consult a doctor

* Please review the disclaimer below.