NDC 70677-1056 Foster And Thrive Chest Congestion Relief Pe PE

View Dosage, Usage, Ingredients, Routes, UNII

Product Information
Product Packages
Product Characteristics
What is NDC 70677-1056?
Foster And Thrive Chest Congestion Relief Pe PE Uses
Active Ingredients UNII Codes
Inactive Ingredients UNII Codes
NDC to RxNorm Crosswalk

Product Information

This product is EXCLUDED from the official NDC directory because the listing certification is expired.

Get all the details for National Drug Code (NDC) 70677-1056 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:

70677-1056

Proprietary Name:

Foster And Thrive Chest Congestion Relief Pe PE

Product Type: [3]

EXPIRED PRODUCT and EXCLUDED from the NDC Directory

Labeler Name: [5]

active Ingredient - (per Tablet)

dextromethorphan Hydrobromide�� 20mg

guaifenesin� 400mg

Labeler Code:

70677

Product Label ID:

3429aedc-e83d-498a-bfca-03aaf5847b3b

FDA Application Number: [6]

M012

Marketing Category: [8]

OTC MONOGRAPH DRUG -

Start Marketing Date: [9]

01-27-2023

Listing Expiration Date: [11]

12-31-2025

Exclude Flag: [12]

Code Navigator:

Product Characteristics

Color(s):

WHITE (C48325)

Shape:

OVAL (C48345)

Size(s):

17 MM

Imprint(s):

RCCGPE;C27

Score:

Code Structure Chart

Product Details

What is NDC 70677-1056?

The NDC code 70677-1056 is assigned by the FDA to the product Foster And Thrive Chest Congestion Relief Pe PE which is product labeled by active Ingredient - (per Tablet)

dextromethorphan Hydrobromide�� 20mg

guaifenesin� 400mg

What are the uses for Foster And Thrive Chest Congestion Relief Pe PE?

■ adults and children 12 years and over:take 1 caplet every 4 hours as needed■ children 6 to under 12 years:take 1/2 caplet every 4 hours as needed■ children under 6 years: consult a doctorDo not exceed 6 doses in a 24 hour period or as directed by a doctor.

Which are Foster And Thrive Chest Congestion Relief Pe PE UNII Codes?

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

GUAIFENESIN (UNII: 495W7451VQ)
GUAIFENESIN (UNII: 495W7451VQ) (Active Moiety)
PHENYLEPHRINE HYDROCHLORIDE (UNII: 04JA59TNSJ)
PHENYLEPHRINE (UNII: 1WS297W6MV) (Active Moiety)

Which are Foster And Thrive Chest Congestion Relief Pe PE 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:

CROSCARMELLOSE SODIUM (UNII: M28OL1HH48)
LACTOSE (UNII: J2B2A4N98G)
MALTODEXTRIN (UNII: 7CVR7L4A2D)
CELLULOSE, MICROCRYSTALLINE (UNII: OP1R32D61U)
MINERAL OIL (UNII: T5L8T28FGP)
POVIDONE (UNII: FZ989GH94E)
MAGNESIUM SILICATE (UNII: 9B9691B2N9)
MAGNESIUM STEARATE (UNII: 70097M6I30)

What is the NDC to RxNorm Crosswalk for Foster And Thrive Chest Congestion Relief Pe PE?

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: 1304111 - guaiFENesin 400 MG / phenylephrine HCl 10 MG Oral Tablet
RxCUI: 1304111 - guaifenesin 400 MG / phenylephrine hydrochloride 10 MG Oral Tablet

* Please review the disclaimer below.

Product Footnotes

[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".

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