NDC 11822-4500 Renewal Anti-dandruff

NDC Product Code 11822-4500

NDC 11822-4500-7

Package Description: 207 mL in 1 BOTTLE, PLASTIC

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

NDC Product Information

Renewal Anti-dandruff with NDC 11822-4500 is a product labeled by Rite Aid Corporation. The generic name of Renewal Anti-dandruff is . The product's dosage form is and is administered via form.

Labeler Name: Rite Aid Corporation

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)
  • SODIUM LAURETH SULFATE (UNII: BPV390UAP0)
  • CARBOMER COPOLYMER TYPE A (ALLYL PENTAERYTHRITOL CROSSLINKED) (UNII: 71DD5V995L)
  • COCO MONOETHANOLAMIDE (UNII: C80684146D)
  • SODIUM COCOYL SARCOSINATE (UNII: 1R9DUY89CZ)
  • GLYCOL DISTEARATE (UNII: 13W7MDN21W)
  • POLYQUATERNIUM-7 (70/30 ACRYLAMIDE/DADMAC; 1600000 MW) (UNII: 0L414VCS5Y)
  • SODIUM CHLORIDE (UNII: 451W47IQ8X)
  • SODIUM HYDROXIDE (UNII: 55X04QC32I)
  • EDETATE SODIUM (UNII: MP1J8420LU)
  • BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K)
  • METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN)
  • METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)
  • FD&C BLUE NO. 1 (UNII: H3R47K3TBD)

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 Corporation
Labeler Code: 11822
Start Marketing Date: 12-08-2014 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 - INACTIVATED, the listing data was inactivated by the FDA. 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 ("Y"), or because the listing certification is expired ("E"), or because the listing data was inactivated by FDA ("I"). Values = "Y", "N", "E", or "I".

* Please review the disclaimer below.

Information for Patients

Salicylic Acid Topical

Salicylic Acid Topical is pronounced as (sal'' i sil' ik as' id)

Why is salicylic acid topical medication prescribed?
Topical salicylic acid is used to help clear and prevent pimples and skin blemishes in people who have acne. Topical salicylic acid is also used to treat skin conditions ...
[Read More]

* Please review the disclaimer below.

Renewal Anti-dandruff Product Label Images

Renewal Anti-dandruff 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

SALICYLIC ACID 2%

Purpose

ANTI-DANDRUFF/ ANTI-SEBORRHEIC DERMATITIS/ ANTI-PSORIASIS

Uses

CONTROLS THE SYMPTOMS OF DANDRUFF, SEBORRHEIC DERMATITIS, AND PSORIASIS

Warnings

FOR EXTERNAL USE ONLY

Ask A Doctor Before Use If You Have

A CONDITION THAT COVERS A LARGE AREA OF THE BODY

When Using This Product

  • AVOID CONTACT WITH EYES. IF CONTACT OCCURS, RINSE EYES THOROUGHLY WITH WATERFOR USE ON COLOR TREATED OR PERMED HAIR, RINSE THOROUGHLY

Stop Use And Ask A Doctor If

CONDITION WORSENS OR DOES NOT IMPROVE AFTER REGULAR USE OF THIS PRODUCT AS DIRECTED

Keep Out Of Reach Of Children

IN CASE OF ACCIDENTAL INGESTION, GET MEDICAL HELP OR CONTACT A POISON CONTROL CENTER IMMEDIATELY

Directions

  • FOR BEST RESULTS, USE TWICE A WEEK OR AS DIRECTED BY A DOCTORWET HAIR, MASSAGE ONTO SCALP FOR SEVERAL MINUTES, AND THEN RINSEREPEAT IF DESIRED

Inactive Ingredients

WATER (AQUA), SODIUM LAURETH SULFATE, ACRYLATES CROSSPOLYMER-4, COCAMIDE MEA, SODIUM COCOYL SARCOSINATE, GLYCOL DISTEARATE, POLYQUATERNIUM-7, FRARANCE (PARFUM), SODIUM CHLORIDE, SODIUM HYDROXIDE, TETRASODIUM EDTA, BHT, METHYLCHLOROISOTHIAZOLINONE, METHYLISOTHIAZOLINONE, BLUE 1 (CI 42090)

* Please review the disclaimer below.