NDC 69008-1032

Natrum Sulph

Natrum Sulphuricum 12x

Natrum Sulph is a Oral Tablet in the Human Otc Drug category. It is labeled and distributed by Warsan Homoeopathic Laboratories. The primary component is Sodium Sulfate.

• Product ID: 69008-1032_6edefce7-e2c0-8a17-e053-2a91aa0a02d0
• NDC: 69008-1032
• Product Type: Human Otc Drug
• Proprietary Name: Natrum Sulph
• Generic Name: Natrum Sulphuricum 12x
• Dosage Form: Tablet
• Route of Administration: ORAL
• Marketing Start Date: 2017-09-07
• Marketing Category: UNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC
• Labeler Name: Warsan Homoeopathic Laboratories
• Substance Name: SODIUM SULFATE
• Active Ingredient Strength: 12 [hp_X]/1
• NDC Exclude Flag: N
• Listing Certified Through: 2019-12-31

Packaging

NDC 69008-1032-1

925 TABLET in 1 BOTTLE, PLASTIC (69008-1032-1)

• Marketing Start Date: 2018-06-17
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 69008-1032-1 [69008103201]

Natrum Sulph TABLET

• Marketing Category: unapproved homeopathic
• Product Type: HUMAN OTC DRUG
• Marketing Start Date: 2018-06-17
• Inactivation Date: 2020-01-31

Drug Details

Active Ingredients

Ingredient	Strength
SODIUM SULFATE	12 [hp_X]/1

OpenFDA Data

• SPL SET ID: 6edefce7-e2c1-8a17-e053-2a91aa0a02d0
• Manufacturer:
  • Warsan Homoeopathic Laboratories
• UNII:
  • 0YPR65R21J

NDC Crossover Matching brand name "Natrum Sulph" or generic name "Natrum Sulphuricum 12x"

NDC	Brand Name	Generic Name
69008-0030	Natrum Sulph	Natrum Sulphuricum
69008-0031	Natrum Sulph	Natrum Sulphuricum
69008-0032	Natrum Sulph	Natrum Sulphuricum 12X
69008-1030	Natrum Sulph	Natrum Sulphuricum
69008-1031	Natrum Sulph	Natrum Sulphuricum
69008-1032	Natrum Sulph	Natrum Sulphuricum 12X
0360-0283	NATRUM SULPHURICUM	NATRUM SULPH
0360-0285	NATRUM SULPHURICUM	NATRUM SULPH