Morning Sickness - Nausea
- Product NDC
- 55714-2379
- 11-digit product format
- 557142379
- Labeler code
- 55714
- Product ID
- 55714-2379_60645c63-bb65-49ea-e053-2a91aa0aeea6
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Bismuthum metallicum, Bryonia, Cimicifuga, Gossypium herbaceum, Ipecac., Kreosotum, Lycopodium, Mag. carb., Nux vom., Pulsatilla, Sepia, Symphoricarpus racemosus, Tabacum, Zingiber, Chamomilla, Hydrastis, Iris versicolor
- Dosage form
- PELLET
- Route
- ORAL
- Labeler
- Newton Laboratories, Inc.
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start
- 2017-04-17
- Marketing end
- 0000-00-00
- Substance
- BISMUTH; BRYONIA ALBA ROOT; BLACK COHOSH; GOSSYPIUM HERBACEUM ROOT BARK; IPECAC; WOOD CREOSOTE; LYCOPODIUM CLAVATUM SPORE; MAGNESIUM CARBONATE; STRYCHNOS NUX-VOMICA SEED; PULSATILLA VULGARIS; SEPIA OFFICINALIS JUICE; SYMPHORICARPOS ALBUS FRUIT; TOBACCO LEAF; GINGER; MATRICARIA RECUTITA; GOLDENSEAL; IRIS VERSICOLOR ROOT
- Active strength
- 15 [hp_X]/g; [hp_X]/g; [hp_X]/g; [hp_X]/g; [hp_X]/g; [hp_X]/g; [hp_X]/g; [hp_X]/g; [hp_X]/g; [hp_X]/g; [hp_X]/g; [hp_X]/g; [hp_X]/g; [hp_X]/g; [hp_X]/g; [hp_X]/g; [hp_X]/g
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- Current FDA listing
- Historical FDA.report record