NDC 53028-1001 Armarita

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:
53028-1001
Proprietary Name:
Armarita
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Jg Select Inc
Labeler Code:
53028
Start Marketing Date: [9]
08-02-2012
Listing Expiration Date: [11]
12-31-2017
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 53028-1001-2

Package Description: 5 SYRINGE, PLASTIC in 1 CARTON / 3 mL in 1 SYRINGE, PLASTIC (53028-1001-1)

Product Details

What is NDC 53028-1001?

The NDC code 53028-1001 is assigned by the FDA to the product Armarita which is product labeled by Jg Select Inc. The product's dosage form is . The product is distributed in a single package with assigned NDC code 53028-1001-2 5 syringe, plastic in 1 carton / 3 ml in 1 syringe, plastic (53028-1001-1). 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 Armarita?

1. after washing your hands, take the product out of the protective wrapper2. snap off the tip to reveal opening3. hold the outer insertion tube where it meets the inner tube, with your thumb and middle finger4. inert the smooth head of the applicator into your vagina until you fingers touch your body (applicator should be about 3 inches inside your vagina)5. push the product inside by pushing the inner tube with your pointer finger all the way in6. remove the applicator, that's it!7. dispose empty applicator in trash

Which are Armarita UNII Codes?

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

Which are Armarita 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".