70565-580 NDC - SAL DE UVAS PICOT ()

Drug Information

  • Product NDC: 70565-580
  • Proprietary Name: Sal de Uvas Picot
  • Non Proprietary Name:
  • Active Ingredient(s):
  • Administration Route(s):
  • Dosage Form(s):

Labeler Information

Field Name Field Value
Labeler Name: Reckitt Benckiser Mexico, S.A. de C.V.
Product Type:
FDA Application Number: part331
Marketing Category: OTC MONOGRAPH FINAL
Start Marketing Date:3/31/2016

Package Information

No. Package Code Package Description Billing Unit
170565-580-016 PACKET in 1 CARTON (70565-580-01) / 1 GRANULE, EFFERVESCENT in 1 PACKET
270565-580-028 PACKET in 1 CARTON (70565-580-02) / 1 GRANULE, EFFERVESCENT in 1 PACKET
370565-580-0312 PACKET in 1 CARTON (70565-580-03) / 1 GRANULE, EFFERVESCENT in 1 PACKET
470565-580-0450 PACKET in 1 CARTON (70565-580-04) / 1 GRANULE, EFFERVESCENT in 1 PACKET

NDC Record

Field Name Field Value Definition
PRODUCT NDC70565-580The 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 NAMESal de Uvas PicotThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
START MARKETING DATE3/31/2016This is the date that the labeler indicates was the start of its marketing of the drug product.
MARKETING CATEGORY NAMEOTC MONOGRAPH 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 NUMBERpart331This 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 NAMEReckitt Benckiser Mexico, S.A. de C.V.Name of Company corresponding to the labeler code segment of the Product NDC.

Download Record

Download this NDC record record in Text format: Export

Download this NDC record record in Excel (CSV) format: Export

Download this NDC record record in XML format: Export

This page was last updated on: 12/19/2025

Previous Code
Next Code