NDC 50845-0017

Vaginitis

Baptisia Tinctoria, Kreosotum, Mercurius Iodatus Ruber, Mercurius Sulphuratus Ruber, Nitricum Acidum, Platinum Metallicum, Sulphur Iodatum, Thymus Suis

Vaginitis is a Oral Spray in the Human Otc Drug category. It is labeled and distributed by Liddell Laboratories, Inc.. The primary component is Baptisia Tinctoria Root; Wood Creosote; Mercuric Iodide; Mercuric Sulfide; Nitric Acid; Platinum; Sulfur Iodide; Sus Scrofa Thymus.

Product ID50845-0017_4c94bef0-0308-4464-91e7-237cb5435f6c
NDC50845-0017
Product TypeHuman Otc Drug
Proprietary NameVaginitis
Generic NameBaptisia Tinctoria, Kreosotum, Mercurius Iodatus Ruber, Mercurius Sulphuratus Ruber, Nitricum Acidum, Platinum Metallicum, Sulphur Iodatum, Thymus Suis
Dosage FormSpray
Route of AdministrationORAL
Marketing Start Date2011-01-13
Marketing End Date2022-07-27
Marketing CategoryUNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC
Labeler NameLiddell Laboratories, Inc.
Substance NameBAPTISIA TINCTORIA ROOT; WOOD CREOSOTE; MERCURIC IODIDE; MERCURIC SULFIDE; NITRIC ACID; PLATINUM; SULFUR IODIDE; SUS SCROFA THYMUS
Active Ingredient Strength3 [hp_X]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_X]/mL
NDC Exclude FlagN

Packaging

NDC 50845-0017-1

30 mL in 1 BOTTLE, SPRAY (50845-0017-1)
Marketing Start Date2011-01-13
Marketing End Date2022-07-27
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 50845-0017-1 [50845001701]

Vaginitis SPRAY
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2011-01-13
Inactivation Date2020-01-31

Drug Details

Active Ingredients

IngredientStrength
BAPTISIA TINCTORIA ROOT3 [hp_X]/mL

OpenFDA Data

SPL SET ID:77b42926-8372-42a5-8c06-d34f151e2a00
Manufacturer
UNII
UPC Code
  • 0363113012965
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