Eczema - Skin Care

Product NDC

55714-2233

11-digit product format

557142233

Labeler code

55714

Product ID

55714-2233_cb6362d0-cacc-9436-ac90-a2a982e15145

Type

HUMAN OTC DRUG

Nonproprietary name

Antimon. crud., Arsenicum alb., Berber. vulg., Bovista, Bryonia, Cantharis, Chelidonium majus, Croton, Dulcamara, Graphites, Hepar sulph. calc., Lycopodium, Mezereum, Nux vom., Petroleum, Pulex irritans, Pulsatilla, Rhus toxicodendron, Sarsaparilla, Sepia, Sulphur iod., Echinacea, Rumex crisp., Taraxacum, Urtica ur.

Dosage form

PELLET

Route

ORAL

Labeler

Newton Laboratories, Inc.

Marketing category

UNAPPROVED HOMEOPATHIC

Marketing start

2011-03-01

Marketing end

0000-00-00

Substance

ANTIMONY TRISULFIDE; ARSENIC TRIOXIDE; BERBERIS VULGARIS ROOT BARK; GIANT PUFFBALL; BRYONIA ALBA ROOT; LYTTA VESICATORIA; CHELIDONIUM MAJUS; CROTON TIGLIUM SEED; SOLANUM DULCAMARA TOP; GRAPHITE; CALCIUM SULFIDE; LYCOPODIUM CLAVATUM SPORE; DAPHNE MEZEREUM BARK; STRYCHNOS NUX-VOMICA SEED; KEROSENE; PULEX IRRITANS; PULSATILLA VULGARIS; TOXICODENDRON PUBESCENS LEAF; SMILAX REGELII ROOT; SEPIA OFFICINALIS JUICE; SULFUR IODIDE; ECHINACEA, UNSPECIFIED; RUMEX CRISPUS ROOT; TARAXACUM OFFICINALE; URTICA URENS

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; [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