Vitiligo
- Product NDC
- 55714-2351
- 11-digit product format
- 557142351
- Labeler code
- 55714
- Product ID
- 55714-2351_ede8eff5-df1c-cb37-bc53-711662e5025d
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Arsenicum alb., Berber. vulg., Bovista, Dolichos, Echinacea, Hura brasiliensis, Hydrocotyle, Lycopodium, Mezereum, Rhus toxicodendron, Rumex crisp., Sepia, Taraxacum,Thuja occ., Urtica ur., Iris versicolor
- Dosage form
- PELLET
- Route
- ORAL
- Labeler
- Newton Laboratories, Inc.
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start
- 2011-03-01
- Marketing end
- 0000-00-00
- Substance
- ARSENIC TRIOXIDE; BERBERIS VULGARIS ROOT BARK; GIANT PUFFBALL; MUCUNA PRURIENS FRUIT TRICHOME; ECHINACEA, UNSPECIFIED; HURA CREPITANS SAP; CENTELLA ASIATICA; LYCOPODIUM CLAVATUM SPORE; DAPHNE MEZEREUM BARK; TOXICODENDRON PUBESCENS LEAF; RUMEX CRISPUS ROOT; SEPIA OFFICINALIS JUICE; TARAXACUM OFFICINALE; THUJA OCCIDENTALIS LEAFY TWIG; URTICA URENS; IRIS VERSICOLOR ROOT
- Active strength
- 10 [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
- 2019-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#