NDC 43406-0629

IODIUM HP

Barium Carbonate, Oyster Shell Calcium Carbonate, Crude, Fucus Vesiculosus, Iodine, Sodium Chloride, Pulsatilla Vulgaris, Spongia Officinalis Skeleton, Roasted, Thyroid

IODIUM HP is a Oral Liquid in the Human Otc Drug category. It is labeled and distributed by Natural Creations, Inc.. The primary component is Barium Carbonate; Fucus Vesiculosus; Iodine; Oyster Shell Calcium Carbonate, Crude; Pulsatilla Vulgaris; Sodium Chloride; Spongia Officinalis Skeleton, Roasted; Thyroid, Unspecified.

Product ID43406-0629_12213eb7-af6b-4e3b-b049-f660cd2b6470
NDC43406-0629
Product TypeHuman Otc Drug
Proprietary NameIODIUM HP
Generic NameBarium Carbonate, Oyster Shell Calcium Carbonate, Crude, Fucus Vesiculosus, Iodine, Sodium Chloride, Pulsatilla Vulgaris, Spongia Officinalis Skeleton, Roasted, Thyroid
Dosage FormLiquid
Route of AdministrationORAL
Marketing Start Date2016-01-01
Marketing CategoryUNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC
Labeler NameNatural Creations, Inc.
Substance NameBARIUM CARBONATE; FUCUS VESICULOSUS; IODINE; OYSTER SHELL CALCIUM CARBONATE, CRUDE; PULSATILLA VULGARIS; SODIUM CHLORIDE; SPONGIA OFFICINALIS SKELETON, ROASTED; THYROID, UNSPECIFIED
Active Ingredient Strength30 [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 Through2023-12-31

Packaging

NDC 43406-0629-1

30 mL in 1 BOTTLE, DROPPER (43406-0629-1)
Marketing Start Date2016-01-01
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 43406-0629-1 [43406062901]

IODIUM HP LIQUID
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2016-01-01
Inactivation Date2020-01-31

Drug Details

Active Ingredients

IngredientStrength
BARIUM CARBONATE30 [hp_X]/mL

OpenFDA Data

SPL SET ID:9353d604-e168-4df1-9726-e965c9fc2c78
Manufacturer
UNII
UPC Code
  • 0877730004673
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