Sal De Uvas Picot Granule, Effervescent
NDC 67751-174

View dosage, usage, ingredients, routes, and UNII mappings.
Table of Contents
  1. Product Information
  2. Product Packages
  3. Product Characteristics
  4. What is NDC 67751-174?
  5. Sal De Uvas Picot Uses
  6. Active Ingredients
  7. Active Ingredients UNII Codes
  8. Inactive Ingredients UNII Codes
  9. NDC to RxNorm Crosswalk
  10. Pharmacologic Classes

Product Information

Sal De Uvas Picot (citric acid monohydrate, sodium bicarbonate) is a OTC MONOGRAPH DRUG-approved product labeled by Navajo Manufacturing Company Inc.. This medication is typically used as a acidifying activity [moa]. It is supplied as a white granule, effervescent for oral administration. This product entry covers the primary NDC 67751-174 and its associated package configuration. This profile includes active and inactive ingredient UNII references and FDA labeling data.

Primary Identification

NDC Product Code:
67751-174
Proprietary Name:
Sal De Uvas Picot
Non-Proprietary Name: [1]
Citric Acid Monohydrate, Sodium Bicarbonate
Substance Name: [2]
Citric Acid Monohydrate; Sodium Bicarbonate
NDC Directory Status:
Human Otc Drug
Product Type: [3]
ACTIVE PRODUCT INCLUDED in the NDC Directory
Code Navigator:

Clinical Specifications

Dosage Form:
Granule, Effervescent - A small particle or grain containing a medicinal agent in a dry mixture usually composed of sodium bicarbonate, citric acid, and tartaric acid which, when in contact with water, has the capability to release gas, resulting in effervescence.
Administration Route(s): [4]
Oral - Administration to or by way of the mouth.

Labeler & Regulatory Data

Labeler Name: [5]
Navajo Manufacturing Company Inc.
Labeler Code:
67751
Product Label ID:
ff6ac79d-564d-4abf-83c7-b01751249c7f
FDA Application Number: [6]
M001
Marketing Category: [8]
OTC MONOGRAPH DRUG

Marketing Timeline

Start Marketing Date: [9]
09-23-2016
Listing Expiration Date: [11]
12-31-2026
Exclude Flag: [12]
N

Product Characteristics

Color(s):
WHITE (C48325)

Code Structure Chart

Product Details

What is NDC 67751-174?

The NDC code 67751-174 is assigned by the FDA to the product Sal De Uvas Picot. It is commonly known by its generic name, citric acid monohydrate, sodium bicarbonate. This pharmaceutical product is labeled by Navajo Manufacturing Company Inc. and is currently categorized as listed product. The medication is a granule, effervescent administered via oral route. In terms of distribution, this product is available in a single package configuration. The associated package NDC(s) include: 67751-174-01. Beyond standard identification, this entry provides technical data including pharmacologic classes, UNII ingredient references, and RxNorm cross-referencing for healthcare systems.

What are the uses of this product?

Fully dissolve one packet in 1/2 glass of water before takingadults 60 years and over 1 packet every 4 hours, or as directed by a doctor. Do not exceed 3 packets in 24 hoursadults and children 12 to 60 years one packet every 4 hours or as directed by a doctor. Do not exceed 4 packets in 24 hourschildren under 12 years  ask a doctor

What are Active Ingredients of this product?

An 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.
  • CITRIC ACID MONOHYDRATE 1.9485 g/1 - A key intermediate in metabolism. It is an acid compound found in citrus fruits. The salts of citric acid (citrates) can be used as anticoagulants due to their calcium chelating ability.
  • SODIUM BICARBONATE 2.485 g/1 - A white, crystalline powder that is commonly used as a pH buffering agent, an electrolyte replenisher, systemic alkalizer and in topical cleansing solutions.

Which are the associated UNII Codes?

The UNII codes for the active ingredients in this product are:

Which are the Inactive Ingredients associated UNII Codes?

The inactive ingredients are all the component of a medicinal product OTHER than the active ingredient(s). The acronym "UNII" stands for “Unique Ingredient Identifier” and is used to identify each inactive ingredient present in a product. The UNII codes for the inactive ingredients in this product are:

What is the NDC to RxNorm Crosswalk for this product?

RxNorm is a normalized naming system for generic and branded drugs that assigns unique concept identifier(s) known as RxCUIs to NDC products.The NDC to RxNorm Crosswalk for this produdct indicates multiple concept unique identifiers (RXCUIs) are associated with this product:
  • RxCUI: 1795948 - citric acid 1.949 GM / sodium bicarbonate 2.485 GM Powder for Oral Solution
  • RxCUI: 1795948 - citric acid 1949 MG / sodium bicarbonate 2485 MG Powder for Oral Solution
  • RxCUI: 1795948 - Citric Acid 1949 MG / NaHCO3 2485 MG Powder for Oral Solution
  • RxCUI: 1795950 - picot 1.949 GM / 2.485 GM Powder for Oral Solution
  • RxCUI: 1795950 - citric acid 1949 MG / sodium bicarbonate 2485 MG Powder for Oral Solution [Picot]

Which are the Pharmacologic Classes of this product?

* Please review the full disclaimer at the bottom of this page.

Product & Regulatory Definitions
What is the Non-Proprietary Name? The non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.
What is the Substance Name? An 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.
What kind of product is this? Indicates 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.
What are the Administration Routes? The translation of the route code submitted by the firm, indicating route of administration.
What is the Labeler Name? Name of Company corresponding to the labeler code segment of the Product NDC.
What is the FDA Application Number? This 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.
What is the Marketing Category? Product 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.
What is the Start Marketing Date? This is the date that the labeler indicates was the start of its marketing of the drug product.
What is the Listing Expiration Date? This is the date when the listing record will expire if not updated or certified by the product labeler.
What is the NDC Exclude Flag? This field indicates whether the product has been removed/excluded from the NDC Directory for failure to respond to FDA"s requests for correction to deficient or non-compliant submissions, or because the listing certification is expired, or because the listing data was inactivated by FDA, or because it was discontinued by the labeler. Possible values in this field are: "D", "E", "I", "N", "U".