NDC 48951-5038 – Helleborus e pl. tota 4

Helleborus Foetidus Root 4 [hp_X]/mL · Liquid · Oral

Human Otc Drug

Product NDC48951-5038

Product details

Brand name
Helleborus e pl. tota 4
Generic name
Helleborus e pl. tota 4
Labeler
Uriel Pharmacy Inc.
Dosage form
Liquid
Route
Oral
Marketing category
UNAPPROVED HOMEOPATHIC
Marketed since
September 1, 2009
Listing expires
December 31, 2027

Active ingredients

Uses, dosage, side effects and warnings for Helleborus e pl. tota 4 →

Package NDC codes (1)

Package NDCDescriptionSince
48951-5038-110 AMPULE in 1 BOX (48951-5038-1) / 1 mL in 1 AMPULESep 1, 2009