NDC 24737-1902 Sundown Honey Soothers Lollipops

View Dosage, Usage, Ingredients, Routes, UNII

Product Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.
NDC Product Code:
24737-1902
Proprietary Name:
Sundown Honey Soothers Lollipops
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
The Nature's Bounty Company
Labeler Code:
24737
Start Marketing Date: [9]
07-01-2019
Listing Expiration Date: [11]
12-31-2020
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Characteristics

Color(s):
ORANGE (C48331)
Shape:
ROUND (C48348)
Size(s):
50 MM
Imprint(s):
NONE
Flavor(s):
RASPBERRY (C73413 - HONEY RASPBERRY)
ORANGE (C73406 - HONEY ORANGE)

Product Packages

NDC Code 24737-1902-2

Package Description: 60 g in 1 CARTON

Product Details

What is NDC 24737-1902?

The NDC code 24737-1902 is assigned by the FDA to the product Sundown Honey Soothers Lollipops which is product labeled by The Nature's Bounty Company. The product's dosage form is . The product is distributed in a single package with assigned NDC code 24737-1902-2 60 g in 1 carton . 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 Sundown Honey Soothers Lollipops?

■ Adults and children 4 years of age and older: Allow product to dissolve slowly in mouth. May be repeated as needed or as directed by a doctor. ■ Children under 4 years of age: Consult a doctor. ■ Adults and children 4 years of age and older: Allow product to dissolve slowly in mouth. May be repeated as needed or as directed by a doctor. ■ Children under 4 years of age: Consult a doctor.

Which are Sundown Honey Soothers Lollipops UNII Codes?

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

Which are Sundown Honey Soothers Lollipops 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

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

[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".