82916-050 NDC - CH6 PERFUMED ALOFORTHYA PEONY AND THE SUNSET (DEXPANTHENOL, SALICYLIC ACID, NIACINAMIDE)

Drug Information

Product NDC: 82916-050

Proprietary Name: CH6 Perfumed Aloforthya Peony and the sunset

Non Proprietary Name: DEXPANTHENOL, SALICYLIC ACID, NIACINAMIDE

Active Ingredient(s):
  • .2 g/100mL DEXPANTHENOL;
  • .1 g/100mL NIACINAMIDE;
  • .2 g/100mL SALICYLIC ACID


Administration Route(s): TOPICAL

Dosage Form(s): SHAMPOO

Labeler Information

Labeler Name: Rea Company
Product Type: HUMAN OTC DRUG
FDA Application Number:
Marketing Category: UNAPPROVED DRUG OTHER
Start Marketing Date:9/1/2022

Package Information

No. Package Code Package Description Billing Unit
182916-050-021 BOTTLE in 1 CARTON (82916-050-02) / 500 mL in 1 BOTTLE (82916-050-01)

NDC Record

Field Name Field Value Definition
PRODUCT NDC82916-050The 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 NAMECH6 Perfumed Aloforthya Peony and the sunsetThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
NON PROPRIETARY NAMEDEXPANTHENOL, SALICYLIC ACID, NIACINAMIDEThe non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.
DOSAGE FORM NAMESHAMPOOThe translation of the dosage form Code submitted by the firm.
ROUTE NAMETOPICALThe translation of the route code submitted by the firm, indicating route of administration.
START MARKETING DATE9/1/2022This is the date that the labeler indicates was the start of its marketing of the drug product.
MARKETING CATEGORY NAMEUNAPPROVED DRUG OTHERProduct 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 NAMERea CompanyName of Company corresponding to the labeler code segment of the Product NDC.
SUBSTANCE NAMEDEXPANTHENOL; NIACINAMIDE; SALICYLIC ACIDAn active ingredient is the substance responsible for the medicinal effects of a product specified by the substance's molecular structure or if the molecular structure is not known, defined by an unambiguous definition that identifies the substance. Each active ingredient name is the preferred term of the UNII code submitted.
ACTIVE NUMERATOR STRENGTH.2; .1; .2 
ACTIVE INGRED UNITg/100mL; g/100mL; g/100mL 

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This page was last updated on: 2/1/2023