NDC 63545-517 Traumacare

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:
63545-517
Proprietary Name:
Traumacare
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Hahnemann Laboratories, Inc. Dba Alpine Pharmaceuticals
Labeler Code:
63545
Start Marketing Date: [9]
06-30-2007
Listing Expiration Date: [11]
12-31-2018
Exclude Flag: [12]
I
Code Navigator:

Product Characteristics

Color(s):
ORANGE (C48331 - ORANGE/PEACH)
Shape:
CAPSULE (C48336)
Size(s):
18 MM
Imprint(s):
TRAUMACARE01
Score:
1

Product Packages

NDC Code 63545-517-01

Package Description: 12 CAPSULE in 1 BLISTER PACK

Product Details

What is NDC 63545-517?

The NDC code 63545-517 is assigned by the FDA to the product Traumacare which is product labeled by Hahnemann Laboratories, Inc. Dba Alpine Pharmaceuticals. The product's dosage form is . The product is distributed in a single package with assigned NDC code 63545-517-01 12 capsule in 1 blister pack . 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 Traumacare?

DirectionsAdults and children 6 years and older. Take one capsule every 8 hours starting as soon as possible after accident, injury, or surgery. For a planned surgery, take one capsule 1-12 hours prior to surgery, then every 8 hours. Do not eat or drink anything for 15 minutes minutes before and after taking TraumaCare. If symptoms persist see your doctor.

Which are Traumacare UNII Codes?

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

Which are Traumacare 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".