NDC 63545-817 Aloe Socotrina

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:
63545-817
Proprietary Name:
Aloe Socotrina
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Hahnemann Laboratories, Inc.
Labeler Code:
63545
Start Marketing Date: [9]
01-13-2020
Listing Expiration Date: [11]
12-31-2021
Exclude Flag: [12]
I
Code Navigator:

Product Characteristics

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

Product Packages

NDC Code 63545-817-01

Package Description: 200 PELLET in 1 VIAL, GLASS

NDC Code 63545-817-02

Package Description: 500 PELLET in 1 VIAL, GLASS

NDC Code 63545-817-03

Package Description: 3000 PELLET in 1 BOTTLE, GLASS

NDC Code 63545-817-04

Package Description: 10000 PELLET in 1 BOTTLE, GLASS

Product Details

What is NDC 63545-817?

The NDC code 63545-817 is assigned by the FDA to the product Aloe Socotrina which is product labeled by Hahnemann Laboratories, Inc.. The product's dosage form is . The product is distributed in 4 packages with assigned NDC codes 63545-817-01 200 pellet in 1 vial, glass , 63545-817-02 500 pellet in 1 vial, glass , 63545-817-03 3000 pellet in 1 bottle, glass , 63545-817-04 10000 pellet in 1 bottle, glass . 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.

Which are Aloe Socotrina UNII Codes?

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

Which are Aloe Socotrina 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:

* 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.

[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".