NDC 68703-007

DeodoRite

Calc Sulph, Carduus Mar, Galium, Mag Phos, Merc Solub, Silicea, Acacia Gum, Lactose, Magnesium Stearate, Starch, Sucrose

DeodoRite is a Oral Tablet in the Human Otc Drug category. It is labeled and distributed by Native Remedies Llc. The primary component is Calcium Sulfate Anhydrous; Silybum Marianum Seed; Galium Aparine; Magnesium Phosphate, Dibasic Trihydrate; Mercurius Solubilis; Silicon Dioxide.

• Product ID: 68703-007_797bb695-f030-42e5-b44a-4d66947aa0e0
• NDC: 68703-007
• Product Type: Human Otc Drug
• Proprietary Name: DeodoRite
• Generic Name: Calc Sulph, Carduus Mar, Galium, Mag Phos, Merc Solub, Silicea, Acacia Gum, Lactose, Magnesium Stearate, Starch, Sucrose
• Dosage Form: Tablet
• Route of Administration: ORAL
• Marketing Start Date: 2013-01-02
• Marketing Category: UNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC
• Labeler Name: Native Remedies LLC
• Substance Name: CALCIUM SULFATE ANHYDROUS; SILYBUM MARIANUM SEED; GALIUM APARINE; MAGNESIUM PHOSPHATE, DIBASIC TRIHYDRATE; MERCURIUS SOLUBILIS; SILICON DIOXIDE
• Active Ingredient Strength: 6 [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_C]/1; [hp_X]/1
• NDC Exclude Flag: E
• Listing Certified Through: 2018-12-31

Packaging

NDC 68703-007-80

180 TABLET in 1 BOTTLE, GLASS (68703-007-80)

• Marketing Start Date: 2013-01-02
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 68703-007-80 [68703000780]

DeodoRite TABLET

• Marketing Category: unapproved homeopathic
• Product Type: HUMAN OTC DRUG
• Marketing Start Date: 2013-01-02
• Inactivation Date: 2020-01-31

Drug Details

Active Ingredients

Ingredient	Strength
CALCIUM SULFATE ANHYDROUS	6 [hp_X]/1

OpenFDA Data

• SPL SET ID: 13fc6c4a-f37d-44df-96f3-c53726d40788
• Manufacturer:
  • Native Remedies LLC
• UNII:
  • E934B3V59H
  • ETJ7Z6XBU4
  • Z4B6561488
  • 324Y4038G2
  • U946SH95EE
  • HF539G9L3Q
• UPC Code:
  • 0810845010757