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NDC 0031-2102 Robitussin Childrens Honey Day Night Dm Value Pack

Dextromethorphan Hbr,Guaifenesin,Doxylamine Succinate Kit - View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. Product Characteristics
  4. What is NDC 0031-2102?
  5. Robitussin Childrens Honey Day Night Dm Value Pack Uses
  6. Active Ingredients UNII Codes
  7. Inactive Ingredients UNII Codes

Product Information

Get all the details for National Drug Code (NDC) 0031-2102 in one place. This page breaks down everything you need to know about the NDC, including proprietary name, active and inactive substances, package configurations, billing units, labeler information, and routes of administration. It also includes enhanced data such as HCPCS codes, FDA product labels with images, UNIIs, and RxNorm cross-references. Whether you're a healthcare professional verifying drug data or a consumer researching medication, this NDC page helps you make informed, accurate decisions.

NDC Product Code:
0031-2102
Proprietary Name:
Robitussin Childrens Honey Day Night Dm Value Pack
Non-Proprietary Name: [1]
Dextromethorphan Hbr, Guaifenesin, Doxylamine Succinate
NDC Directory Status:
Human Otc Drug
Product Type: [3]
ACTIVE PRODUCT INCLUDED in the NDC Directory
Dosage Form:
Kit - A packaged collection of related material.
Labeler Name: [5]
Haleon Us Holdings Llc
Labeler Code:
0031
Product Label ID:
f9999875-3433-4052-a628-39539d373216
FDA Application Number: [6]
M012
Marketing Category: [8]
OTC MONOGRAPH DRUG -
Start Marketing Date: [9]
05-27-2019
Listing Expiration Date: [11]
12-31-2026
Exclude Flag: [12]
N
Code Navigator:

Product Characteristics

Flavor(s):
BERRY (C73365)

Code Structure Chart

Product Details

What is NDC 0031-2102?

The NDC code 0031-2102 is assigned by the FDA to the product Robitussin Childrens Honey Day Night Dm Value Pack which is a human over the counter drug product labeled by Haleon Us Holdings Llc. The generic name of Robitussin Childrens Honey Day Night Dm Value Pack is dextromethorphan hbr, guaifenesin, doxylamine succinate. The product's dosage form is kit. The product is distributed in a single package with assigned NDC code 0031-2102-01 1 kit in 1 carton * 1 bottle in 1 carton (0031-8760-12) / 118 ml in 1 bottle * 1 bottle in 1 carton (0031-8762-12) / 118 ml in 1 bottle. This page includes all the important details about this product, including active and inactive ingredients, pharmagologic classes, product uses and characteristics, UNII information and RxNorm crosswalk.

What are the uses for Robitussin Childrens Honey Day Night Dm Value Pack?

▪do not take more than 6 doses in any 24-hour period▪measure only with dosing cup provided▪keep dosing cup with product▪mL = milliliteragedosechildren under 4 yearsdo not usechildren 4 to under 6 years5 mL every 4 hourschildren 6 to under 12 years10 mL every 4 hoursadults and children 12 years and over20 mL every 4 hours

Which are Robitussin Childrens Honey Day Night Dm Value Pack UNII Codes?

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

Which are Robitussin Childrens Honey Day Night Dm Value Pack Inactive Ingredients 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:

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Product Footnotes

[1] 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.

[3] 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.

[5] What is the Labeler Name? - Name of Company corresponding to the labeler code segment of the Product NDC.

[6] 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.

[8] 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.

[9] What is the Start Marketing Date? - This is the date that the labeler indicates was the start of its marketing of the drug product.

[11] 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.

[12] 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".