NDC 70965-002

Womens PLATINUM

Calcarea Carbonica, Capsicum Annuum, Ferrum Metallicum, Glandula Suprarenalis, Graphites, Hepar Suis, Hypothalamus, Iodium, Kali Carbonicum, Oophorinum, Pancreatinum, Phytolacca Decandra, Pulsatilla, Sepia.

Womens PLATINUM is a Oral Liquid in the Human Otc Drug category. It is labeled and distributed by Breakthrough M2 Inc. The primary component is Oyster Shell Calcium Carbonate, Crude; Capsicum; Iron; Sus Scrofa Adrenal Gland; Graphite; Pork Liver; Bos Taurus Hypothalamus; Iodine; Potassium Carbonate; Sus Scrofa Ovary; Pancrelipase; Phytolacca Americana Root; Pulsatilla Vulgaris; Sepia Officinalis Juice.

• Product ID: 70965-002_d9b2b5dd-c304-4dd4-883d-4b3529b58d82
• NDC: 70965-002
• Product Type: Human Otc Drug
• Proprietary Name: Womens PLATINUM
• Generic Name: Calcarea Carbonica, Capsicum Annuum, Ferrum Metallicum, Glandula Suprarenalis, Graphites, Hepar Suis, Hypothalamus, Iodium, Kali Carbonicum, Oophorinum, Pancreatinum, Phytolacca Decandra, Pulsatilla, Sepia.
• Dosage Form: Liquid
• Route of Administration: ORAL
• Marketing Start Date: 2016-10-10
• Marketing Category: UNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC
• Labeler Name: Breakthrough M2 Inc
• Substance Name: OYSTER SHELL CALCIUM CARBONATE, CRUDE; CAPSICUM; IRON; SUS SCROFA ADRENAL GLAND; GRAPHITE; PORK LIVER; BOS TAURUS HYPOTHALAMUS; IODINE; POTASSIUM CARBONATE; SUS SCROFA OVARY; PANCRELIPASE; PHYTOLACCA AMERICANA ROOT; PULSATILLA VULGARIS; SEPIA OFFICINALIS JUICE
• Active Ingredient Strength: 12 [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL
• NDC Exclude Flag: N
• Listing Certified Through: 2020-12-31

Packaging

NDC 70965-002-02

59 mL in 1 BOTTLE, DROPPER (70965-002-02)

• Marketing Start Date: 2016-10-10
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 70965-002-02 [70965000202]

Womens PLATINUM LIQUID

• Marketing Category: unapproved homeopathic
• Product Type: HUMAN OTC DRUG
• Marketing Start Date: 2016-10-10

Drug Details

Active Ingredients

Ingredient	Strength
OYSTER SHELL CALCIUM CARBONATE, CRUDE	12 [hp_X]/59mL

OpenFDA Data

• SPL SET ID: bb65a25a-6c5b-4773-8eed-b08cd76348d4
• Manufacturer:
  • Breakthrough M2 Inc
• UNII:
  • S7YTV04R8O
  • BQN1B9B9HA
  • S6G2NLH4Y7
  • I76KB35JEV
  • 4QQN74LH4O
  • QDL83WN8C2
  • 9679TC07X4
  • E1UOL152H7
  • 398IYQ16YV
  • 00UK7646FG
  • 2E32821G6I
  • 11E6VI8VEG
  • FQ3DRG0N5K
  • 6EC706HI7F