| PRODUCT NDC | 63083-2147 | 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. |
| PRODUCT TYPE NAME | HUMAN OTC DRUG | 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. |
| PROPRIETARY NAME | Attention Deficit Severe Drops | The proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes. |
| PROPRIETARY NAME SUFFIX | 2147 | 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. |
| NON PROPRIETARY NAME | Attention Deficit Severe Drops | The non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product. |
| DOSAGE FORM NAME | LIQUID | The translation of the dosage form Code submitted by the firm. |
| ROUTE NAME | ORAL | The translation of the route code submitted by the firm, indicating route of administration. |
| START MARKETING DATE | 8/15/1984 | This is the date that the labeler indicates was the start of its marketing of the drug product. |
| MARKETING CATEGORY NAME | UNAPPROVED HOMEOPATHIC | 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. |
| LABELER NAME | Professional Complementary Health Formulas | Name of Company corresponding to the labeler code segment of the Product NDC. |
| SUBSTANCE NAME | .GAMMA.-AMINOBUTYRIC ACID; AMARYLLIS BELLADONNA WHOLE; AMBERGRIS; BARIUM CARBONATE; BARIUM CHLORIDE DIHYDRATE; BEEF KIDNEY; BEEF LIVER; BOS TAURUS BRAIN; BOS TAURUS HYPOTHALAMUS; BOS TAURUS PANCREAS; BOVINE TUBERCULIN; BUFO BUFO CUTANEOUS GLAND; COFFEA ARABICA SEED, ROASTED; DATURA STRAMONIUM; GINKGO; GONORRHEAL URETHRAL SECRETION HUMAN; HYOSCYAMUS NIGER; INSULIN GLULISINE; LYCOPODIUM CLAVATUM SPORE; LYCOSA TARANTULA; PHOSPHORUS; SILVER NITRATE; SUS SCROFA PINEAL GLAND; THUJA OCCIDENTALIS LEAF; VERATRUM ALBUM ROOT | An active ingredient is the substance responsible for the medicinal effects of a product specified by the substance's molecular structure or if the molecular structure is not known, defined by an unambiguous definition that identifies the substance. Each active ingredient name is the preferred term of the UNII code submitted. |
| ACTIVE NUMERATOR STRENGTH | 3; 60; 60; 60; 60; 6; 6; 6; 6; 6; 60; 60; 30; 60; 3; 60; 60; 60; 30; 60; 60; 30; 6; 60; 60 | |
| ACTIVE INGRED UNIT | [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL | |
| PHARM CLASSES | Allergens [CS], Cell-mediated Immunity [PE], Dietary Proteins [CS], Increased Histamine Release [PE], Insulin Analog [EPC], Insulin [Chemical/Ingredient], Meat Proteins [EXT], Non-Standardized Food Allergenic Extract [EPC] | |