57955-9994 NDC - 911 ADRENAL BURNOUT AND FATIGUE (ACETICUM AC, ADRENALINUM, ADRENOCORTICOTROPHIN (30X), AESCULUS HIPPOCASTANUM, FLOS, ALFALFA, ALPHA-LIPOIC AC, AMBRA, ARG NIT, AVENA SATIVA, BRYONIA, CARBONEUM OXYGENISATUM, CARPINUS BETULUS, FLOS, DNA, FUMARICUM ACIDUM, GELSEMIUM SEMPERVIRENS, HEPAR SULPHURIS CALCAREUM, HYPOTHALAMUS, KALI PHOSPHORICUM, LACTICUM ACIDUM, LECITHIN, NATRUM MURIATICUM, OXALICUM ACIDUM, PHOSPHORICUM ACIDUM, PITUITARUM POSTERIUM, SARCOLACTICUM ACIDUM, SELENIUM METALLICUM, SEPIA, SILICEA, SUCCINICUM ACIDUM AND THYROIDINUM.)

Drug Information

  • Product NDC: 57955-9994
  • Proprietary Name: 911 Adrenal Burnout and Fatigue
  • Non Proprietary Name: Aceticum ac, Adrenalinum, Adrenocorticotrophin (30X), Aesculus hippocastanum, flos, Alfalfa, Alpha-lipoic ac, Ambra, Arg nit, Avena sativa, Bryonia, Carboneum oxygenisatum, Carpinus betulus, flos, DNA, Fumaricum acidum, Gelsemium sempervirens, Hepar sulphuris calcareum, Hypothalamus, Kali phosphoricum, Lacticum acidum, Lecithin, Natrum muriaticum, Oxalicum acidum, Phosphoricum acidum, Pituitarum posterium, Sarcolacticum acidum, Selenium metallicum, Sepia, Silicea, Succinicum acidum and Thyroidinum.
  • Active Ingredient(s): 10 [hp_X]/59mL ACETIC ACID; 10 [hp_X]/59mL AESCULUS HIPPOCASTANUM FLOWER; 10 [hp_X]/59mL ALFALFA; 10 [hp_X]/59mL ALPHA LIPOIC ACID; 10 [hp_X]/59mL AMBERGRIS; 10 [hp_X]/59mL AVENA SATIVA FLOWERING TOP; 10 [hp_X]/59mL BOS TAURUS HYPOTHALAMUS; 10 [hp_X]/59mL BRYONIA ALBA ROOT; 10 [hp_X]/59mL CALCIUM SULFIDE; 10 [hp_X]/59mL CARBON MONOXIDE; 10 [hp_X]/59mL CARPINUS BETULUS FLOWERING TOP; 30 [hp_X]/59mL CORTICOTROPIN; 10 [hp_X]/59mL DIBASIC POTASSIUM PHOSPHATE; 10 [hp_X]/59mL EGG PHOSPHOLIPIDS; 10 [hp_X]/59mL EPINEPHRINE; 10 [hp_X]/59mL FUMARIC ACID; 10 [hp_X]/59mL GELSEMIUM SEMPERVIRENS ROOT; 10 [hp_X]/59mL HERRING SPERM DNA; 10 [hp_X]/59mL LACTIC ACID, DL-; 10 [hp_X]/59mL LACTIC ACID, L-; 10 [hp_X]/59mL OXALIC ACID DIHYDRATE; 10 [hp_X]/59mL PHOSPHORIC ACID; 10 [hp_X]/59mL SELENIUM; 10 [hp_X]/59mL SEPIA OFFICINALIS JUICE; 10 [hp_X]/59mL SILICON DIOXIDE; 10 [hp_X]/59mL SILVER NITRATE; 10 [hp_X]/59mL SODIUM CHLORIDE; 10 [hp_X]/59mL SUCCINIC ACID; 10 [hp_X]/59mL SUS SCROFA PITUITARY GLAND, POSTERIOR; 10 [hp_X]/59mL THYROID, UNSPECIFIED
  • Administration Route(s): ORAL
  • Dosage Form(s): LIQUID
  • Pharmacy Class(es): Adrenergic alpha-Agonists [MoA]; Adrenergic beta-Agonists [MoA]; Adrenocorticotropic Hormone [CS]; Adrenocorticotropic Hormone [EPC]; Catecholamine [EPC]; Catecholamines [CS]; alpha-Adrenergic Agonist [EPC]; beta-Adrenergic Agonist [EPC]

Labeler Information

Field Name Field Value
Labeler Name: King Bio Inc.
Product Type: HUMAN OTC DRUG
FDA Application Number:
Marketing Category: UNAPPROVED HOMEOPATHIC
Start Marketing Date:10/8/2025

Package Information

No. Package Code Package Description Billing Unit
157955-9994-259 mL in 1 BOTTLE, SPRAY (57955-9994-2)

NDC Record

Field Name Field Value Definition
PRODUCT NDC57955-9994The 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 NAMEHUMAN OTC DRUGIndicates 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 NAME911 Adrenal Burnout and FatigueThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
NON PROPRIETARY NAMEAceticum ac, Adrenalinum, Adrenocorticotrophin (30X), Aesculus hippocastanum, flos, Alfalfa, Alpha-lipoic ac, Ambra, Arg nit, Avena sativa, Bryonia, Carboneum oxygenisatum, Carpinus betulus, flos, DNA, Fumaricum acidum, Gelsemium sempervirens, Hepar sulphuris calcareum, Hypothalamus, Kali phosphoricum, Lacticum acidum, Lecithin, Natrum muriaticum, Oxalicum acidum, Phosphoricum acidum, Pituitarum posterium, Sarcolacticum acidum, Selenium metallicum, Sepia, Silicea, Succinicum acidum and 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 NAMELIQUIDThe translation of the dosage form Code submitted by the firm.
ROUTE NAMEORALThe translation of the route code submitted by the firm, indicating route of administration.
START MARKETING DATE10/8/2025This is the date that the labeler indicates was the start of its marketing of the drug product.
MARKETING CATEGORY NAMEUNAPPROVED HOMEOPATHICProduct 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 NAMEKing Bio Inc.Name of Company corresponding to the labeler code segment of the Product NDC.
SUBSTANCE NAMEACETIC ACID; AESCULUS HIPPOCASTANUM FLOWER; ALFALFA; ALPHA LIPOIC ACID; AMBERGRIS; AVENA SATIVA FLOWERING TOP; BOS TAURUS HYPOTHALAMUS; BRYONIA ALBA ROOT; CALCIUM SULFIDE; CARBON MONOXIDE; CARPINUS BETULUS FLOWERING TOP; CORTICOTROPIN; DIBASIC POTASSIUM PHOSPHATE; EGG PHOSPHOLIPIDS; EPINEPHRINE; FUMARIC ACID; GELSEMIUM SEMPERVIRENS ROOT; HERRING SPERM DNA; LACTIC ACID, DL-; LACTIC ACID, L-; OXALIC ACID DIHYDRATE; PHOSPHORIC ACID; SELENIUM; SEPIA OFFICINALIS JUICE; SILICON DIOXIDE; SILVER NITRATE; SODIUM CHLORIDE; SUCCINIC ACID; SUS SCROFA PITUITARY GLAND, POSTERIOR; THYROID, UNSPECIFIEDAn 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 STRENGTH10; 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 
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 
PHARM CLASSESAdrenergic alpha-Agonists [MoA], Adrenergic beta-Agonists [MoA], Adrenocorticotropic Hormone [CS], Adrenocorticotropic Hormone [EPC], Catecholamine [EPC], Catecholamines [CS], alpha-Adrenergic Agonist [EPC], beta-Adrenergic Agonist [EPC] 

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This page was last updated on: 12/6/2025

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