NDC 44911-0474

Age Defiance Pro

7-oxo-dehydroepiandrosterone-3b-acetate, Calcarea Carbonica, Conium Maculatum, Glandula Suprarenalis Suis, Hepar Suis, Hydrofluoricum Acidum, Hypophysis Suis, Lycopodium Clavatum, Selenium Metallicum, Sepia, Silicea, Human Growth Hormone

Age Defiance Pro is a Oral Liquid in the Human Otc Drug category. It is labeled and distributed by Energique, Inc.. The primary component is 7-oxodehydroepiandrosterone 3-acetate; Oyster Shell Calcium Carbonate, Crude; Conium Maculatum Flowering Top; Sus Scrofa Adrenal Gland; Pork Liver; Hydrofluoric Acid; Sus Scrofa Pituitary Gland; Lycopodium Clavatum Spore; Selenium; Sepia Officinalis Juice; Silicon Dioxide; Somatropin.

Product ID44911-0474_195115ec-c462-4f4f-8b9d-86c81ea0e527
NDC44911-0474
Product TypeHuman Otc Drug
Proprietary NameAge Defiance Pro
Generic Name7-oxo-dehydroepiandrosterone-3b-acetate, Calcarea Carbonica, Conium Maculatum, Glandula Suprarenalis Suis, Hepar Suis, Hydrofluoricum Acidum, Hypophysis Suis, Lycopodium Clavatum, Selenium Metallicum, Sepia, Silicea, Human Growth Hormone
Dosage FormLiquid
Route of AdministrationORAL
Marketing Start Date2018-09-24
Marketing CategoryUNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC
Labeler NameEnergique, Inc.
Substance Name7-OXODEHYDROEPIANDROSTERONE 3-ACETATE; OYSTER SHELL CALCIUM CARBONATE, CRUDE; CONIUM MACULATUM FLOWERING TOP; SUS SCROFA ADRENAL GLAND; PORK LIVER; HYDROFLUORIC ACID; SUS SCROFA PITUITARY GLAND; LYCOPODIUM CLAVATUM SPORE; SELENIUM; SEPIA OFFICINALIS JUICE; SILICON DIOXIDE; SOMATROPIN
Active Ingredient Strength12 [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_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL
NDC Exclude FlagN
Listing Certified Through2020-12-31

Packaging

NDC 44911-0474-1

30 mL in 1 BOTTLE, DROPPER (44911-0474-1)
Marketing Start Date2018-09-24
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 44911-0474-1 [44911047401]

Age Defiance Pro LIQUID
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-09-24

Drug Details

Active Ingredients

IngredientStrength
7-OXODEHYDROEPIANDROSTERONE 3-ACETATE12 [hp_X]/mL

OpenFDA Data

SPL SET ID:d528bdbe-fb75-4b13-9cbc-efa2177d74d8
Manufacturer
UNII

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