NDC 15631-2315 Graphites
NDC Product 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.
Non-Proprietary Name: What is the Non-Proprietary Name?
The non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.
NDC Code Structure
- 15631 - Rxhomeo Private Limited D.b.a. Rxhomeo, Inc
- 15631-2315 - Graphites
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
NDC Product Information
Graphites with NDC 15631-2315 is a product labeled by Rxhomeo Private Limited D.b.a. Rxhomeo, Inc. The generic name of Graphites is . The product's dosage form is and is administered via form.
Labeler Name: Rxhomeo Private Limited D.b.a. Rxhomeo, Inc
Dosage Form: -
Product Type: What kind of product is this?
Indicates the type of product, such as Human Prescription Drug or Human Over the Counter Drug. This data element matches the “Document Type” field of the Structured Product Listing.
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 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. Values = ‘Y’ or ‘N’.
* 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
- Uses
- Indications
- Dosage & Administration Section
- Warnings
- Otc - Stop Use
- Otc - Pregnancy Or Breast Feeding
- Otc - Keep Out Of Reach Of Children
- Otc - Do Not Use
- Inactive Ingredients
- Storage
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.