11822-2234 NDC - 2 TO 12 YEARS CHILDRENS COLD AND MUCUS (EUPHRASIA STRICTA,SILICON DIOXIDE, RUMEX CRISPUS ROOT, ANEMONE PULSATILLA, GOLDENSEAL, SODIUM CHLORIDE, PHOSPHORUS, ONION, BRYONIA ALBA ROOT, MATRICARIA CHAMOMILLA, ARABICA COFFEE BEAN, CALCIUM SULFIDE AND SULFUR)

Drug Information

  • Product NDC: 11822-2234
  • Proprietary Name: 2 to 12 YEARS CHILDRENS COLD and MUCUS
  • Non Proprietary Name: euphrasia stricta,silicon dioxide, rumex crispus root, anemone pulsatilla, goldenseal, sodium chloride, phosphorus, onion, bryonia alba root, matricaria chamomilla, arabica coffee bean, calcium sulfide and sulfur
  • Active Ingredient(s):
  • Administration Route(s):
  • Dosage Form(s): KIT

Labeler Information

Field Name Field Value
Labeler Name: Rite Aid Hdgrts Corp
Product Type: HUMAN OTC DRUG
FDA Application Number:
Marketing Category: UNAPPROVED HOMEOPATHIC
Start Marketing Date:12/29/2021

Package Information

No. Package Code Package Description Billing Unit
111822-2234-11 KIT in 1 CARTON (11822-2234-1) * 1 BOTTLE in 1 CARTON (11822-2245-4) / 118 mL in 1 BOTTLE * 1 BOTTLE in 1 CARTON (11822-1245-4) / 118 mL in 1 BOTTLE

NDC Record

Field Name Field Value Definition
PRODUCT NDC11822-2234The labeler code and product code segments of the National Drug Code number, separated by a hyphen. Asterisks are no longer used or included within the product code segment to indicate certain configurations of the NDC.
PRODUCT TYPE NAMEHUMAN OTC DRUGIndicates 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.
PROPRIETARY NAME2 to 12 YEARS CHILDRENS COLD and MUCUSThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
NON PROPRIETARY NAMEeuphrasia stricta,silicon dioxide, rumex crispus root, anemone pulsatilla, goldenseal, sodium chloride, phosphorus, onion, bryonia alba root, matricaria chamomilla, arabica coffee bean, calcium sulfide and sulfurThe non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.
DOSAGE FORM NAMEKITThe translation of the dosage form Code submitted by the firm.
START MARKETING DATE12/29/2021This is the date that the labeler indicates was the start of its marketing of the drug product.
MARKETING CATEGORY NAMEUNAPPROVED HOMEOPATHICProduct types are broken down into several potential Marketing Categories, such as NDA/ANDA/BLA, OTC Monograph, or Unapproved Drug. One and only one Marketing Category may be chosen for a product, not all marketing categories are available to all product types. Currently, only final marketed product categories are included. The complete list of codes and translations can be found at www.fda.gov/edrls under Structured Product Labeling Resources.
LABELER NAMERite Aid Hdgrts CorpName of Company corresponding to the labeler code segment of the Product NDC.

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This page was last updated on: 12/6/2025

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