NDC 61096-0031 Sprayology Pms Support

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:
61096-0031
Proprietary Name:
Sprayology Pms Support
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Eight And Company
Labeler Code:
61096
Start Marketing Date: [9]
03-10-2014
Listing Expiration Date: [11]
12-31-2018
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 61096-0031-1

Package Description: 1 BOTTLE, SPRAY in 1 CARTON / 41 mL in 1 BOTTLE, SPRAY

Product Details

What is NDC 61096-0031?

The NDC code 61096-0031 is assigned by the FDA to the product Sprayology Pms Support which is product labeled by Eight And Company. The product's dosage form is . The product is distributed in a single package with assigned NDC code 61096-0031-1 1 bottle, spray in 1 carton / 41 ml in 1 bottle, spray. 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 Sprayology Pms Support?

Temporarily relieves common symptoms of pre-menstrual syndrome, including:° cramps° emotional fluctuations° fluid retention° irregular menstruation° natural° gluten free° no artificial flavors or colors° no known negative drug interactions

Which are Sprayology Pms Support UNII Codes?

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

Which are Sprayology Pms Support 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".