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  4. NDC Product Code: 54973-3307 Baby Tiny Cold Daytime And Nighttime

NDC 54973-3307 Baby Tiny Cold Daytime And Nighttime

Eupatorium Perfoliatum Flowering Top,Euphrasia Stricta,Gelsemium Sempervirens - View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. Product Characteristics
  4. What is NDC 54973-3307?
  5. Baby Tiny Cold Daytime And Nighttime Uses
  6. Active Ingredients UNII Codes
  7. Inactive Ingredients UNII Codes

Product Information

NDC Product Code:
54973-3307
Proprietary Name:
Baby Tiny Cold Daytime And Nighttime
Non-Proprietary Name: [1]
Eupatorium Perfoliatum Flowering Top, Euphrasia Stricta, Gelsemium Sempervirens Root, Potassium Iodide, And Matricaria Recutita
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]
Hyland's Inc.
Labeler Code:
54973
Product Label ID:
be7cff09-ecff-48bd-96d4-dc7d47db7656
Marketing Category: [8]
UNAPPROVED HOMEOPATHIC - A category specifying that a product is marketed as unapproved homeopathic product.
Start Marketing Date: [9]
01-11-2017
Listing Expiration Date: [11]
12-31-2024
Exclude Flag: [12]
N
Code Navigator:

Product Characteristics

Color(s):
WHITE (C48325)
Shape:
ROUND (C48348)
Size(s):
5 MM
Score:
1

Code Structure Chart

Product Details

What is NDC 54973-3307?

The NDC code 54973-3307 is assigned by the FDA to the product Baby Tiny Cold Daytime And Nighttime which is a human over the counter drug product labeled by Hyland's Inc.. The generic name of Baby Tiny Cold Daytime And Nighttime is eupatorium perfoliatum flowering top, euphrasia stricta, gelsemium sempervirens root, potassium iodide, and matricaria recutita. The product's dosage form is kit. The product is distributed in a single package with assigned NDC code 54973-3307-1 1 kit in 1 carton * 1 bottle, plastic in 1 carton (54973-3158-1) / 125 tablet, soluble in 1 bottle, plastic * 1 bottle, plastic in 1 carton (54973-3252-1) / 125 tablet in 1 bottle, plastic. 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 Baby Tiny Cold Daytime And Nighttime?

Children under 6 months of age: consult a licensed health care professional before using this product.Children 6 months to 1 year of age: dissolve 2 tablets on tongue every 15 minutes for 4 doses, then hourly until relieved.Children 1 to 3 years of age: dissolve 3 tablets on tongue every 15 minutes for 4 doses, then hourly until relieved.Hyland's Baby Tiny Cold Tablets are very soft and will dissolve almost instantly in the mouth. Children under 6 months of age: consult a licensed health care professional before using this product.Children 6 months to 1 year of age: dissolve 2 tablets on tongue every 4 hours during the night as required.Children 1 to 3 years of age: dissolve 3 tablets on tongue every 4 hours during the night as required.Hyland's Baby Nighttime Tiny Cold Tablets are very soft and will dissolve almost instantly in the mouth.

Which are Baby Tiny Cold Daytime And Nighttime UNII Codes?

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

  • EUPATORIUM PERFOLIATUM FLOWERING TOP (UNII: 1W0775VX6E)
  • EUPATORIUM PERFOLIATUM FLOWERING TOP (UNII: 1W0775VX6E) (Active Moiety)
  • EUPHRASIA STRICTA (UNII: C9642I91WL)
  • EUPHRASIA STRICTA (UNII: C9642I91WL) (Active Moiety)
  • GELSEMIUM SEMPERVIRENS ROOT (UNII: 639KR60Q1Q)
  • GELSEMIUM SEMPERVIRENS ROOT (UNII: 639KR60Q1Q) (Active Moiety)
  • POTASSIUM IODIDE (UNII: 1C4QK22F9J)
  • IODIDE ION (UNII: 09G4I6V86Q) (Active Moiety)
  • MATRICARIA RECUTITA (UNII: G0R4UBI2ZZ)
  • MATRICARIA RECUTITA (UNII: G0R4UBI2ZZ) (Active Moiety)

Which are Baby Tiny Cold Daytime And Nighttime 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.

[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 ("Y"), or because the listing certification is expired ("E"), or because the listing data was inactivated by FDA ("I"). Values = "Y", "N", "E", or "I".