Estrogen and Progesterone
- Product NDC
- 43853-0001
- 11-digit product format
- 438530001
- Labeler code
- 43853
- Product ID
- 43853-0001_8cc56347-a99b-4a87-8684-96dca3ad9761
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Agnus Castus, Angelica Sinensis, Apis Mellifica, Arnica Montana, Cimicifuga Racemosa, Estradiol, Estriol, Folliculinum, Galium Aparine, Glycyrrhiza Glabra, Korean Ginseng, Oophorinum (Suis), Progesterone, Sepia, Thuja Occidentalis, Viscum Album
- Dosage form
- SPRAY
- Route
- ORAL
- Labeler
- ProBLEN
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start
- 2014-02-05
- Marketing end
- 2020-12-21
- Substance
- CHASTE TREE; ANGELICA SINENSIS ROOT; APIS MELLIFERA; ARNICA MONTANA; BLACK COHOSH; ESTRADIOL; ESTRIOL; ESTRONE; GALIUM APARINE; GLYCYRRHIZA GLABRA; ASIAN GINSENG; SUS SCROFA OVARY; PROGESTERONE; SEPIA OFFICINALIS JUICE; THUJA OCCIDENTALIS LEAF; VISCUM ALBUM FRUITING TOP
- Active strength
- 3 [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_C]/mL; [hp_X]/mL; [hp_C]/mL; [hp_X]/mL; [hp_X]/mL
- NDC exclude flag
- No
- Listing certified through
- 0000-00-00
- Current FDA listing
- Historical FDA.report record