NDC 49726-009

Viratrol Herpes Symptom Relief

Apis Mellifica, Arsenicum Album, Borax, Capsicum Annuum, Graphites, Mentha Piperita, Mezereum, Natrum Muriaticum, Nux Vomica, Petroleum, Ranunculus Bulbosus

Viratrol Herpes Symptom Relief is a Oral; Topical Liquid in the Human Otc Drug category. It is labeled and distributed by Hello Life, Inc.. The primary component is Apis Mellifera; Arsenic Trioxide; Sodium Borate; Capsicum; Graphite; Peppermint; Daphne Mezereum Bark; Sodium Chloride; Strychnos Nux-vomica Seed; Paraffin; Ranunculus Bulbosus; Toxicodendron Pubescens Leaf.

Product ID49726-009_7df0a51f-ea79-754b-e053-2991aa0a5e6c
NDC49726-009
Product TypeHuman Otc Drug
Proprietary NameViratrol Herpes Symptom Relief
Generic NameApis Mellifica, Arsenicum Album, Borax, Capsicum Annuum, Graphites, Mentha Piperita, Mezereum, Natrum Muriaticum, Nux Vomica, Petroleum, Ranunculus Bulbosus
Dosage FormLiquid
Route of AdministrationORAL; TOPICAL
Marketing Start Date2010-01-07
Marketing CategoryUNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC
Labeler NameHello Life, Inc.
Substance NameAPIS MELLIFERA; ARSENIC TRIOXIDE; SODIUM BORATE; CAPSICUM; GRAPHITE; PEPPERMINT; DAPHNE MEZEREUM BARK; SODIUM CHLORIDE; STRYCHNOS NUX-VOMICA SEED; PARAFFIN; RANUNCULUS BULBOSUS; TOXICODENDRON PUBESCENS LEAF
Active Ingredient Strength10 [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 FlagN
Listing Certified Through2019-12-31

Packaging

NDC 49726-009-02

1 BOTTLE in 1 CARTON (49726-009-02) > 59 mL in 1 BOTTLE
Marketing Start Date2010-01-07
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 49726-009-02 [49726000902]

Viratrol Herpes Symptom Relief LIQUID
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2010-01-07
Inactivation Date2020-01-31

Drug Details


Trademark Results [Viratrol]

Mark Image

Registration | Serial
Company
Trademark
Application Date
VIRATROL
VIRATROL
75101023 2124324 Live/Registered
NEXMED (U.S.A.), INC.
1996-05-07

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