NDC 43853-0008

Adrenal and DHEA

Aralia Quinquefolia, Arnica Montana, Avena Sativa, Carduus Marianus, Dhea, Glandula Suprarenalis Suis, L-arginine

Adrenal and DHEA is a Oral Liquid in the Human Otc Drug category. It is labeled and distributed by Problen. The primary component is American Ginseng; Arnica Montana; Avena Sativa Flowering Top; Silybum Marianum Seed; Prasterone; Sus Scrofa Adrenal Gland; Arginine; Sodium Chloride; Phosphoric Acid; Thuja Occidentalis Leaf; .alpha.-tocopherol.

• Product ID: 43853-0008_3992ec41-9aae-4e88-83be-6032a43e5d77
• NDC: 43853-0008
• Product Type: Human Otc Drug
• Proprietary Name: Adrenal and DHEA
• Generic Name: Aralia Quinquefolia, Arnica Montana, Avena Sativa, Carduus Marianus, Dhea, Glandula Suprarenalis Suis, L-arginine
• Dosage Form: Liquid
• Route of Administration: ORAL
• Marketing Start Date: 2013-04-23
• Marketing Category: UNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC
• Labeler Name: ProBLEN
• Substance Name: AMERICAN GINSENG; ARNICA MONTANA; AVENA SATIVA FLOWERING TOP; SILYBUM MARIANUM SEED; PRASTERONE; SUS SCROFA ADRENAL GLAND; ARGININE; SODIUM CHLORIDE; PHOSPHORIC ACID; THUJA OCCIDENTALIS LEAF; .ALPHA.-TOCOPHEROL
• Active Ingredient Strength: 3 [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_C]/mL; [hp_C]/mL; [hp_X]/mL
• NDC Exclude Flag: N
• Listing Certified Through: 2019-12-31

Packaging

NDC 43853-0008-3

1 CARTON in 1 CARTON (43853-0008-3) > 1 BOTTLE, SPRAY in 1 CARTON (43853-0008-2) > 30 mL in 1 BOTTLE, SPRAY (43853-0008-1)

• Marketing Start Date: 2013-04-23
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 43853-0008-2 [43853000802]

Adrenal and DHEA LIQUID

• Marketing Category: unapproved homeopathic
• Product Type: HUMAN OTC DRUG
• Marketing Start Date: 2013-04-23

NDC 43853-0008-1 [43853000801]

Adrenal and DHEA LIQUID

• Marketing Category: unapproved homeopathic
• Product Type: HUMAN OTC DRUG
• Marketing Start Date: 2013-04-23

NDC 43853-0008-3 [43853000803]

Adrenal and DHEA LIQUID

• Marketing Category: unapproved homeopathic
• Product Type: HUMAN OTC DRUG
• Marketing Start Date: 2013-04-23
• Inactivation Date: 2020-01-31

Drug Details

Active Ingredients

Ingredient	Strength
AMERICAN GINSENG	3 [hp_X]/mL

OpenFDA Data

• SPL SET ID: c0718768-6f1f-43c2-8c91-e6c94af9d089
• Manufacturer:
  • ProBLEN
• UNII:
  • MA9CQJ3F7F
  • O80TY208ZW
  • 94ZLA3W45F
  • 459AG36T1B
  • 451W47IQ8X
  • 398IYQ16YV
  • 8W75VCV53Q
  • 0T0DQN8786
  • H4N855PNZ1
  • E4GA8884NN
  • U946SH95EE

NDC Crossover Matching brand name "Adrenal and DHEA" or generic name "Aralia Quinquefolia, Arnica Montana, Avena Sativa, Carduus Marianus, Dhea, Glandula Suprarenalis Suis, L-arginine"

NDC	Brand Name	Generic Name
43853-0008	Adrenal and DHEA	Aralia Quinquefolia, Arnica Montana, Avena Sativa, Carduus Marianus, Dhea, Glandula Suprarenalis Suis, L-Arginine
43853-0020	Adrenal and DHEA	Aralia Quinquefolia, Ashwagandha, Avena Sativa, Carduus Marianus, Dhea, Glandula Suprarenalis Suis, L-Arginine, Natrum Muriaticum, Phosphoricum Acidum, Rhodiola.
50845-0086	Adrenal and DHEA	Aralia quinquefolia, Arnica montana, Avena sativa, Carduus marianus, DHEA, Glandula suprarenalis suis, L-arginine, Natrum muriaticum, Phosphoricum acidum, Thuja occidentalis, Vitamin E,