NDC 48951-8434 – Sun Pyrite 17X

Ferrous Disulfide 17 [hp_X]/mL · Liquid · Oral

Human Otc Drug

Product NDC48951-8434

Product details

Brand name
Sun Pyrite 17X
Generic name
Sun Pyrite 17X
Labeler
Uriel Pharmacy, Inc
Dosage form
Liquid
Route
Oral
Marketing category
UNAPPROVED HOMEOPATHIC
Marketed since
September 1, 2009
Listing expires
December 31, 2026

Active ingredients

Uses, dosage, side effects and warnings for Sun Pyrite 17X →

Package NDC codes (1)

Package NDCDescriptionSince
48951-8434-360 mL in 1 BOTTLE, DROPPER (48951-8434-3)Sep 1, 2009