Amethyst Rosa

Product NDC

48951-1271

11-digit product format

489511271

Labeler code

48951

Product ID

48951-1271_69829f45-0821-8a34-e053-2991aa0acab6

Type

HUMAN OTC DRUG

Nonproprietary name

Amethyst Rosa

Dosage form

CAPSULE

Route

ORAL

Labeler

Uriel Pharmacy Inc.

Marketing category

UNAPPROVED HOMEOPATHIC

Marketing start

2009-09-01

Marketing end

0000-00-00

Substance

SILICON DIOXIDE; ACTIVATED CHARCOAL; FUMARIA OFFICINALIS FLOWERING TOP; WORMWOOD; BETULA PUBESCENS LEAF; ACORUS CALAMUS ROOT; MATRICARIA RECUTITA; COCHLEARIA OFFICINALIS FLOWERING TOP; GENTIANA LUTEA ROOT; GEUM URBANUM ROOT; OXALIS ACETOSELLA LEAF; ROSA RUGOSA FLOWER BUD; URTICA DIOICA LEAF; URTICA DIOICA ROOT; GINGER; ANTIMONY TRISULFIDE; BLACK PEPPER; FERRIC OXIDE RED; GRAPHITE

Active strength

2 [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1

NDC exclude flag

No

Listing certified through

2020-12-31

Current FDA listing

Historical FDA.report record