11673-635 NDC - CALAMINE PLUS PRAMOXINE HCL (CALAMINE PLUS SPRAY)

Drug Information

Product NDC: 11673-635

Proprietary Name: Calamine Plus Pramoxine HCl

Non Proprietary Name: Calamine Plus Spray

Active Ingredient(s):
  • .345 mg/116g FERRIC OXIDE RED;
  • 2.72 mg/116g PRAMOXINE HYDROCHLORIDE;
  • 24.16 mg/116g ZINC OXIDE


Administration Route(s): TOPICAL

Dosage Form(s): AEROSOL, SPRAY

Pharmacy Class(es):
  • Copper Absorption Inhibitor [EPC];
  • Decreased Copper Ion Absorption [PE]

Labeler Information

Labeler Name: Target Corporation
Product Type: HUMAN OTC DRUG
FDA Application Number: part348
Marketing Category: OTC MONOGRAPH NOT FINAL
Start Marketing Date:2/1/2018

Package Information

No. Package Code Package Description Billing Unit
111673-635-41116 g in 1 CANISTER (11673-635-41)

NDC Record

Field Name Field Value Definition
PRODUCT NDC11673-635The 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 NAMECalamine Plus Pramoxine HClThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
NON PROPRIETARY NAMECalamine Plus SprayThe non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.
DOSAGE FORM NAMEAEROSOL, SPRAYThe 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 DATE2/1/2018This is the date that the labeler indicates was the start of its marketing of the drug product.
MARKETING CATEGORY NAMEOTC MONOGRAPH NOT FINALProduct 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.
APPLICATION NUMBERpart348This corresponds to the NDA, ANDA, or BLA number reported by the labeler for products which have the corresponding Marketing Category designated. If the designated Marketing Category is OTC Monograph Final or OTC Monograph Not Final, then the Application number will be the CFR citation corresponding to the appropriate Monograph (e.g. “part 341”). For unapproved drugs, this field will be null.
LABELER NAMETarget CorporationName of Company corresponding to the labeler code segment of the Product NDC.
SUBSTANCE NAMEFERRIC OXIDE RED; PRAMOXINE HYDROCHLORIDE; ZINC OXIDEAn 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.345; 2.72; 24.16 
ACTIVE INGRED UNITmg/116g; mg/116g; mg/116g 
PHARM CLASSESCopper Absorption Inhibitor [EPC], Decreased Copper Ion Absorption [PE] 

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