NDC 15631-2315 Graphites

  1. Labeler Index
  2. Rxhomeo Private Limited D.b.a. Rxhomeo, Inc
  3. NDC: 15631-2315 Graphites

NDC Product Code 15631-2315

NDC CODE: 15631-2315

Proprietary Name: Graphites What is the Proprietary Name?
The proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.

NDC Code Structure

NDC 15631-2315-0

Package Description: 1 CONTAINER in 1 CONTAINER > 50 g in 1 CONTAINER

NDC 15631-2315-1

Package Description: 1 CONTAINER in 1 CONTAINER > 100 g in 1 CONTAINER

NDC 15631-2315-2

Package Description: 1 CONTAINER in 1 CONTAINER > 200 g in 1 CONTAINER

NDC 15631-2315-3

Package Description: 1 CONTAINER in 1 CONTAINER > 500 g in 1 CONTAINER

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.

NDC Product Information

Graphites with NDC 15631-2315 is product labeled by Rxhomeo Private Limited D.b.a. Rxhomeo, Inc. The product's dosage form is and is administered via form.

Inactive Ingredient(s)

About the Inactive Ingredient(s)
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.
  • ALOE VERA LEAF (UNII: ZY81Z83H0X)

Product Labeler Information

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

Labeler Name: Rxhomeo Private Limited D.b.a. Rxhomeo, Inc
Labeler Code: 15631
Start Marketing Date: 03-30-2016 What is the Start Marketing Date?
This is the date that the labeler indicates was the start of its marketing of the drug product.
Listing Expiration Date: 12-31-2018 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.
Exclude Flag: I - INACTIVATED, the listing data was inactivated by the FDA. 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".

* Please review the disclaimer below.

Graphites Product Label Images

Graphites Product Labeling Information

The product labeling information includes all published material associated to a drug. Product labeling documents include information like generic names, active ingredients, ingredient strength dosage, routes of administration, appearance, usage, warnings, inactive ingredients, etc.

Product Labeling Index

Active Ingredient

GRAPHITES GEL 1X HPUS

Uses

Eczema, acne vulgaris, keloid scars

Indications

Condition listed above or as directed by the physician

Dosage & Administration Section

Apply a thin layer of Gel to the affected area, repeat 3 times a day or as needed.

Warnings

This product is to be used for self-limiting conditions

Otc - Stop Use

If symptoms do not improve in 4 days, or worsen, discontinue use and seek assistance of health professional

Otc - Pregnancy Or Breast Feeding

As with any drug, if you are preganant, or nursing a baby, seek professional advice before taking this product

Otc - Keep Out Of Reach Of Children

Keep this and all medication out of reach of children

Otc - Do Not Use

Do not use if capseal is broken or missing.Close the cap tightly after use.

Inactive Ingredients

ALOE VERA GEL

Storage

Store in a cool dark place

* Please review the disclaimer below.