Cellergy with NDC 71753-8099 is a a human over the counter drug product labeled by Ratis, Llc. The generic name of Cellergy is calcarea fluorica, calcarea phosphorica, calcarea sulphurica, ferrum phosphoricum, kali muriaticum, kali phosphoricum, kali sulphuricum, magnesia phosphorica, natrum muriaticum, natrum phosphoricum, natrum sulphuricum, silicea.. The product's dosage form is liquid and is administered via oral form.
Labeler Name: Ratis, Llc
Dosage Form: Liquid - A dosage form consisting of a pure chemical in its liquid1 state. This dosage form term should not be applied to solutions.
Product Type: Human Otc Drug 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.
Cellergy Active Ingredient(s) What is the Active Ingredient(s) List?
This is the active ingredient list. Each ingredient name is the preferred term of the UNII code submitted.
- CALCIUM FLUORIDE 12 [hp_X]/mL
- TRIBASIC CALCIUM PHOSPHATE 12 [hp_X]/mL
- CALCIUM SULFATE ANHYDROUS 12 [hp_X]/mL
- FERROSOFERRIC PHOSPHATE 12 [hp_X]/mL
- POTASSIUM CHLORIDE 12 [hp_X]/mL
- DIBASIC POTASSIUM PHOSPHATE 12 [hp_X]/mL
- POTASSIUM SULFATE 12 [hp_X]/mL
- MAGNESIUM PHOSPHATE, DIBASIC TRIHYDRATE 12 [hp_X]/mL
- SODIUM CHLORIDE 12 [hp_X]/mL
- SODIUM PHOSPHATE, DIBASIC, HEPTAHYDRATE 12 [hp_X]/mL
- SODIUM SULFATE 12 [hp_X]/mL
- SILICON DIOXIDE 12 [hp_X]/mL
Administration Route(s) What are the Administration Route(s)?
The translation of the route code submitted by the firm, indicating route of administration.
- Oral - Administration to or by way of the mouth.
Product Labeler Information What is the Labeler Name?
Name of Company corresponding to the labeler code segment of the Product NDC.
Labeler Name: Ratis, Llc
Labeler Code: 71753
Marketing Category: UNAPPROVED HOMEOPATHIC - What is the Marketing Category?
Product types are broken down into several potential Marketing Categories, such as NDA/ANDA/BLA, OTC Monograph, or Unapproved Drug. One and only one Marketing Category may be chosen for a product, not all marketing categories are available to all product types. Currently, only final marketed product categories are included. The complete list of codes and translations can be found at www.fda.gov/edrls under Structured Product Labeling Resources.
Start Marketing Date: 10-08-2019 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: 12-31-2020 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: N 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.