| PRODUCT NDC | 57955-9001 | 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 | 911 Adrenal Burnout and Fatigue | 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 | Aceticum ac, Adrenalinum, Adrenocorticotrophin, Aesculus hipp, flos, Alfalfa, Alpha-lipoic ac, Ambra, Argentum nitricum, Avena, Bryonia, Carboneum oxygenisatum, Carpinus betulus, flos, Citricum ac, DNA, Fumaricum ac, Gelsemium, Hepar sulph culc, Hypothalamus suis, Kali phos, Lacticum ac, Lecithin, Nat mur, Oxalicum acidum, Phosphoricum acidum, Pituitarum posterium, Sarcolacticum acidum, Selenium metallicum, Sepia, Silicea, Succinicum acidum, Thyroidinum | 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 | 6/22/2022 | 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 | King Bio Inc. | Name of Company corresponding to the labeler code segment of the Product NDC. |
| SUBSTANCE NAME | ACETIC ACID; AESCULUS HIPPOCASTANUM FLOWER; ALPHA LIPOIC ACID; AMBERGRIS; ANHYDROUS CITRIC ACID; APRINOCARSEN; AVENA SATIVA FLOWERING TOP; BRYONIA ALBA ROOT; CALCIUM SULFIDE; CARBON MONOXIDE; CARPINUS BETULUS FLOWERING TOP; CORTICOTROPIN; DIBASIC POTASSIUM PHOSPHATE; EPINEPHRINE; FUMARIC ACID; GELSEMIUM SEMPERVIRENS ROOT; HERRING SPERM DNA; LACTIC ACID, DL-; LACTIC ACID, L-; MEDICAGO SATIVA WHOLE; OXALIC ACID DIHYDRATE; PHOSPHORIC ACID; SELENIUM; SEPIA OFFICINALIS JUICE; SILICON DIOXIDE; SILVER NITRATE; SODIUM CHLORIDE; SUCCINIC ACID; SUS SCROFA HYPOTHALAMUS; SUS SCROFA PITUITARY GLAND, POSTERIOR; THYROID, UNSPECIFIED | 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 | 10; 10; 10; 10; 10; 10; 10; 10; 10; 10; 10; 30; 10; 10; 10; 10; 10; 10; 10; 10; 10; 10; 10; 10; 10; 10; 10; 10; 10; 10; 10 | |
| 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; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL | |
| PHARM CLASSES | Acidifying Activity [MoA], Adrenergic alpha-Agonists [MoA], Adrenergic beta-Agonists [MoA], Adrenocorticotropic Hormone [CS], Adrenocorticotropic Hormone [EPC], Anti-coagulant [EPC], Calcium Chelating Activity [MoA], Calculi Dissolution Agent [EPC], Catecholamine [EPC], Catecholamines [CS], Decreased Coagulation Factor Activity [PE], alpha-Adrenergic Agonist [EPC], beta-Adrenergic Agonist [EPC] | |