NDC 66096-184

OHM Dermatological Terrain

Calcarea Carbonica, Calcarea Fluorica, Carduus Marianus, China Officinalis, Cynara Scolymus, Galium Aparine, Graphites, Hepar Sulphuris Calcareum, Manganum Phosphoricum, Nicotinamidum, Oleander, Taraxacum Officinale, Thuja Occidentalis.

OHM Dermatological Terrain is a Oral Liquid in the Human Otc Drug category. It is labeled and distributed by Ohm Pharma Inc.. The primary component is Oyster Shell Calcium Carbonate, Crude; Calcium Fluoride; Milk Thistle; Cinchona Officinalis Bark; Cynara Scolymus Leaf; Galium Aparine; Graphite; Calcium Sulfide; Manganese Phosphate, Dibasic; Niacinamide; Nerium Oleander Leaf; Taraxacum Officinale; Thuja Occidentalis Leafy Twig.

Product ID66096-184_b8a696d0-66ee-0db7-e053-2a95a90abeb5
NDC66096-184
Product TypeHuman Otc Drug
Proprietary NameOHM Dermatological Terrain
Generic NameCalcarea Carbonica, Calcarea Fluorica, Carduus Marianus, China Officinalis, Cynara Scolymus, Galium Aparine, Graphites, Hepar Sulphuris Calcareum, Manganum Phosphoricum, Nicotinamidum, Oleander, Taraxacum Officinale, Thuja Occidentalis.
Dosage FormLiquid
Route of AdministrationORAL
Marketing Start Date2015-04-13
Marketing CategoryUNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC
Labeler NameOHM PHARMA INC.
Substance NameOYSTER SHELL CALCIUM CARBONATE, CRUDE; CALCIUM FLUORIDE; MILK THISTLE; CINCHONA OFFICINALIS BARK; CYNARA SCOLYMUS LEAF; GALIUM APARINE; GRAPHITE; CALCIUM SULFIDE; MANGANESE PHOSPHATE, DIBASIC; NIACINAMIDE; NERIUM OLEANDER LEAF; TARAXACUM OFFICINALE; THUJA OCCIDENTALIS LEAFY TWIG
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; [hp_X]/mL
NDC Exclude FlagN
Listing Certified Through2022-12-31

Packaging

NDC 66096-184-06

12 AMPULE in 1 BOX (66096-184-06) > 2.2 mL in 1 AMPULE
Marketing Start Date2015-04-13
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 66096-184-06 [66096018406]

OHM Dermatological Terrain LIQUID
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2015-04-13

Drug Details

Active Ingredients

IngredientStrength
OYSTER SHELL CALCIUM CARBONATE, CRUDE12 [hp_X]/mL

OpenFDA Data

SPL SET ID:d2a45a96-5e0e-4d00-832f-3acfb2ab82de
Manufacturer
UNII
UPC Code
  • 0366096016241
  • 0366096184063

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