| Drug NDC: | 63083-7534 |
| The labeler code and product code segments of the National Drug Code number, separated by a hyphen. Asterisks are no longer used or included within the product code segment to indicate certain configurations of the NDC. | |
| Proprietary Name: | Weight Management Formula 7534 |
| Also known as the trade name. It is the name of the product chosen by the labeler. | |
| Proprietary Name Base: | Weight Management Formula |
| The base of the Brand/Proprietary name excluding its suffix. | |
| Proprietary Name Suffix: | 7534 |
| A suffix to the proprietary name, a value here should be appended to the ProprietaryName field to obtain the complete name of the product. This suffix is often used to distinguish characteristics of a product such as extended release (“XR”) or sleep aid (“PM”). Although many companies follow certain naming conventions for suffices, there is no recognized standard. | |
| Product Type: | Human Otc Drug |
| Indicates the type of product, such as Human Prescription Drug or Human OTC Drug. This data element corresponds to the “Document Type” of the SPL submission for the listing. | |
| Non Proprietary Name: | Weight Management Formula |
| Also known as the generic name, this is usually the active ingredient(s) of the product. | |
| Labeler Name: | Professional Complementary Health Formulas |
| Name of Company corresponding to the labeler code segment of the ProductNDC. | |
| Dosage Form: | Liquid |
| The translation of the DosageForm Code submitted by the firm. There is no standard, but values may include terms like `tablet` or `solution for injection`.The complete list of codes and translations can be found www.fda.gov/edrls under Structured Product Labeling Resources. | |
| Status: | Active |
| FDA does not review and approve unfinished products. Therefore, all products in this file are considered unapproved. | |
| Substance Name: | ALPHA LIPOIC ACID - 3 [hp_X]/59mL AMMONIUM BROMIDE - 12 [hp_X]/59mL AMMONIUM CARBONATE - 6 [hp_X]/59mL ANTIMONY TRISULFIDE - 8 [hp_X]/59mL ARTEMISIA CINA PRE-FLOWERING TOP - 3 [hp_X]/59mL BOS TAURUS HYPOTHALAMUS - 6 [hp_X]/59mL BOS TAURUS PITUITARY GLAND, POSTERIOR - 6 [hp_X]/59mL DELPHINIUM STAPHISAGRIA SEED - 6 [hp_X]/59mL FUCUS VESICULOSUS - 3 [hp_X]/59mL GARCINIA GUMMI-GUTTA FRUIT - 2 [hp_X]/59mL Load more... LYCOPODIUM CLAVATUM SPORE - 12 [hp_X]/59mL NERIUM OLEANDER WHOLE - 6 [hp_X]/59mL OLEA EUROPAEA FLOWER - 30 [hp_X]/59mL OYSTER SHELL CALCIUM CARBONATE, CRUDE - 30 [hp_X]/59mL PHOSPHORUS - 6 [hp_X]/59mL SEMECARPUS ANACARDIUM JUICE - 6 [hp_X]/59mL SODIUM CHLORIDE - 6 [hp_X]/59mL THYROID, UNSPECIFIED - 6 [hp_X]/59mL |
| This is the active ingredient list. Each ingredient name is the preferred term of the UNII code submitted. | |
| Route Details: | ORAL |
| The translation of the Route Code submitted by the firm, indicating route of administration. The complete list of codes and translations can be found at www.fda.gov/edrls under Structured Product Labeling Resources. | |
| Marketing Category: | UNAPPROVED HOMEOPATHIC |
| Product types are broken down into several potential Marketing Categories, such as New Drug Application (NDA), Abbreviated New Drug Application (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. | |
| Marketing Start Date: | 15 Aug, 1984 |
| This is the date that the labeler indicates was the start of its marketing of the drug product. | |
| Marketing End Date: | 10 Jun, 2026 |
| This is the date the product will no longer be available on the market. If a product is no longer being manufactured, in most cases, the FDA recommends firms use the expiration date of the last lot produced as the EndMarketingDate, to reflect the potential for drug product to remain available after manufacturing has ceased. Products that are the subject of ongoing manufacturing will not ordinarily have any EndMarketingDate. Products with a value in the EndMarketingDate will be removed from the NDC Directory when the EndMarketingDate is reached. | |
| Listing Expiration Date: | 31 Dec, 2023 |
| This is the date when the listing record will expire if not updated or certified by the firm. | |
| Manufacturer Name: | Professional Complementary Health Formulas |
| Name of manufacturer or company that makes this drug product, corresponding to the labeler code segment of the NDC. | |
| Original Packager: | Yes |
| Whether or not the drug has been repackaged for distribution. | |
| UNII: | 73Y7P0K73Y R0JB3224WS NJ5VT0FKLJ F79059A38U 28M1820ACT S6G2NLH4Y7 7JM57I419K 00543AP1JV 535G2ABX9M D0QJI8UQVR Load more... C88X29Y479 JG9V5H8412 498M34P1VZ 2E32821G6I 27YLU75U4W Y0F0BU8RDU 451W47IQ8X 0B4FDL9I6P |
| Unique Ingredient Identifier, which is a non-proprietary, free, unique, unambiguous, non-semantic, alphanumeric identifier based on a substance’s molecular structure and/or descriptive information. | |
| Package NDC | Description | Marketing Start Date | Marketing End Date | Sample Available |
|---|---|---|---|---|
| 63083-7534-2 | 59 mL in 1 BOTTLE, DROPPER (63083-7534-2) | 15 Aug, 1985 | N/A | No |
| Package NDC number, known as the NDC, identifies the labeler, product, and trade package size. The first segment, the labeler code, is assigned by the FDA. Description tells the size and type of packaging in sentence form. Multilevel packages will have the descriptions concatenated together. | ||||
* Data of this site is collected from www.fda.gov. This page is for informational purposes only. Always consult your physician with any questions you may have regarding a medical condition.