57900-002 NDC - COLD HOT PATCH ()

Drug Information

  • Product NDC: 57900-002
  • Proprietary Name: cold hot patch
  • Non Proprietary Name:
  • Active Ingredient(s):
  • Administration Route(s):
  • Dosage Form(s):

Labeler Information

Field Name Field Value
Labeler Name: Zhejiang Bangli Medical Products CO.,LTD
Product Type:
FDA Application Number: part348
Marketing Category: OTC MONOGRAPH NOT FINAL
Start Marketing Date:3/18/2014

Package Information

No. Package Code Package Description Billing Unit
157900-002-014 PACKAGE in 1 CARTON (57900-002-01) / 12 BOX in 1 PACKAGE / 1 BAG in 1 BOX / 2 PATCH in 1 BAG / .408 g in 1 PATCH
257900-002-023 PACKAGE in 1 CARTON (57900-002-02) / 12 BOX in 1 PACKAGE / 6 BAG in 1 BOX / 1 PATCH in 1 BAG / .408 g in 1 PATCH
357900-002-034 PACKAGE in 1 CARTON (57900-002-03) / 12 BOX in 1 PACKAGE / 1 BAG in 1 BOX / 3 PATCH in 1 BAG / .408 g in 1 PATCH
457900-002-0450 BOX in 1 CARTON (57900-002-04) / 1 BAG in 1 BOX / 5 PATCH in 1 BAG / .408 g in 1 PATCH
557900-002-0548 BOX in 1 CARTON (57900-002-05) / 3 BAG in 1 BOX / 1 PATCH in 1 BAG / .408 g in 1 PATCH
657900-002-068 PACKAGE in 1 CARTON (57900-002-06) / 6 BOX in 1 PACKAGE / 1 BAG in 1 BOX / 5 PATCH in 1 BAG / .408 g in 1 PATCH
757900-002-074 PACKAGE in 1 CARTON (57900-002-07) / 6 BOX in 1 PACKAGE / 1 BAG in 1 BOX / 5 PATCH in 1 BAG / .408 g in 1 PATCH
857900-002-084 PACKAGE in 1 CARTON (57900-002-08) / 50 BOX in 1 PACKAGE / 1 BAG in 1 BOX / 5 PATCH in 1 BAG / .85 g in 1 PATCH
957900-002-0930 BOX in 1 CARTON (57900-002-09) / 1 BAG in 1 BOX / 5 PATCH in 1 BAG / .595 g in 1 PATCH
1057900-002-108 PACKAGE in 1 CARTON (57900-002-10) / 6 BOX in 1 PACKAGE / 1 BAG in 1 BOX / 5 PATCH in 1 BAG / .595 g in 1 PATCH
1157900-002-114 PACKAGE in 1 CARTON (57900-002-11) / 6 BOX in 1 PACKAGE / 1 BAG in 1 BOX / 5 PATCH in 1 BAG / .595 g in 1 PATCH
1257900-002-128 PACKAGE in 1 CARTON (57900-002-12) / 6 BOX in 1 PACKAGE / 1 BAG in 1 BOX / 3 PATCH in 1 BAG / 1.487 g in 1 PATCH

NDC Record

Field Name Field Value Definition
PRODUCT NDC57900-002The 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.
PROPRIETARY NAMEcold hot patchThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
START MARKETING DATE3/18/2014This 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 NAMEZhejiang Bangli Medical Products CO.,LTDName of Company corresponding to the labeler code segment of the Product NDC.

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This page was last updated on: 11/21/2025

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