NDC 15631-0640 Natrum Phosphoricum
NDC Product Code 15631-0640
Proprietary Name: Natrum Phosphoricum 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 15631-0640-0
Package Description: 1 TABLET in 1 BLISTER PACK
NDC 15631-0640-1
Package Description: 4 TABLET in 1 BLISTER PACK
NDC 15631-0640-2
Package Description: 50 TABLET in 1 CONTAINER
NDC 15631-0640-3
Package Description: 100 TABLET in 1 CONTAINER
NDC 15631-0640-4
Package Description: 250 TABLET in 1 CONTAINER
NDC 15631-0640-5
Package Description: 500 TABLET in 1 CONTAINER
NDC 15631-0640-6
Package Description: 1000 TABLET in 1 CONTAINER
NDC 15631-0640-7
Package Description: 10000 TABLET in 1 CONTAINER
NDC Product Information
Natrum Phosphoricum with NDC 15631-0640 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.
- LACTOSE (UNII: J2B2A4N98G)
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: 12-07-2015 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.
Natrum Phosphoricum Product Label Images
Natrum Phosphoricum 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
- 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
NATRUM PHOSPHORICUM HPUS 1X and Higher
Uses
Hyperacidity, Mouth Ulcers
Indications
Condition listed above or as directed by the physician
Dosage
Adults- Take 4 or 6 Tablets by mouth, three times daily or as suggested by physician. Children 2 years and older- take 1/2 the adult dose.
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 pregnant, 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
Lactose
Storage
Store in a cool dark place
* Please review the disclaimer below.