NDC 49726-002

Activive Fatigue Symptom Relief

Alfalfa, Ambra Grisea, Anacardium Orientale, Argentum Nitricum, Aurum Metalicum, Avena Sativa, Caladium Seguinum, Calcarea Carbonica, Cocculus Indicus, Gelsemium Sempervirens, Ignatia Amara, Kali Phosphoricum, Lycopodium Clavatum, Natrum Muriaticum, Nux Vomica, Phosphoricum Acidum, Phosphorus, Selenium Metallicum, Sepia, Silicea, Sulphur

Activive Fatigue Symptom Relief is a Oral Liquid in the Human Otc Drug category. It is labeled and distributed by Hello Life, Inc.. The primary component is Alfalfa; Ambergris; Semecarpus Anacardium Juice; Silver Nitrate; Gold; Avena Sativa Flowering Top; Dieffenbachia Seguine; Oyster Shell Calcium Carbonate, Crude; Anamirta Cocculus Seed; Gelsemium Sempervirens Root; Strychnos Ignatii Seed; Potassium Phosphate, Dibasic; Lycopodium Clavatum Spore; Sodium Chloride; Strychnos Nux-vomica Seed; Phosphoric Acid; Phosphorus; Selenium; Sepia Officinalis Juice; Silicon Dioxide; Sulfur.

• Product ID: 49726-002_7e03a372-e1ca-8f0d-e053-2a91aa0ae739
• NDC: 49726-002
• Product Type: Human Otc Drug
• Proprietary Name: Activive Fatigue Symptom Relief
• Generic Name: Alfalfa, Ambra Grisea, Anacardium Orientale, Argentum Nitricum, Aurum Metalicum, Avena Sativa, Caladium Seguinum, Calcarea Carbonica, Cocculus Indicus, Gelsemium Sempervirens, Ignatia Amara, Kali Phosphoricum, Lycopodium Clavatum, Natrum Muriaticum, Nux Vomica, Phosphoricum Acidum, Phosphorus, Selenium Metallicum, Sepia, Silicea, Sulphur
• Dosage Form: Liquid
• Route of Administration: ORAL
• Marketing Start Date: 2010-01-07
• Marketing Category: UNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC
• Labeler Name: Hello Life, Inc.
• Substance Name: ALFALFA; AMBERGRIS; SEMECARPUS ANACARDIUM JUICE; SILVER NITRATE; GOLD; AVENA SATIVA FLOWERING TOP; DIEFFENBACHIA SEGUINE; OYSTER SHELL CALCIUM CARBONATE, CRUDE; ANAMIRTA COCCULUS SEED; GELSEMIUM SEMPERVIRENS ROOT; STRYCHNOS IGNATII SEED; POTASSIUM PHOSPHATE, DIBASIC; LYCOPODIUM CLAVATUM SPORE; SODIUM CHLORIDE; STRYCHNOS NUX-VOMICA SEED; PHOSPHORIC ACID; PHOSPHORUS; SELENIUM; SEPIA OFFICINALIS JUICE; SILICON DIOXIDE; SULFUR
• Active Ingredient Strength: 10 [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
• NDC Exclude Flag: N
• Listing Certified Through: 2019-12-31

Packaging

NDC 49726-002-02

1 BOTTLE in 1 CARTON (49726-002-02) > 59 mL in 1 BOTTLE

• Marketing Start Date: 2010-01-07
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 49726-002-02 [49726000202]

Activive Fatigue Symptom Relief LIQUID

• Marketing Category: unapproved homeopathic
• Product Type: HUMAN OTC DRUG
• Marketing Start Date: 2010-01-07
• Inactivation Date: 2020-01-31

Drug Details

Active Ingredients

Ingredient	Strength
ALFALFA	10 [hp_X]/59mL

OpenFDA Data

• SPL SET ID: 6692ac64-b411-4adc-83c3-921693f3d4e1
• Manufacturer:
  • Hello Life, Inc.
• UNII:
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