FDA.reportPublic FDA data

Formica 7X Special Order

Manufacturer
Uriel Pharmacy Inc.
Effective date
2018-07-09
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-02 00:53:35

Label at a glance#

ProductFormica 7X Special Order
Active ingredientFORMICA RUFA
Label structure1 sections

Label contents#

Full prescribing information#

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Formica 7 Special Order AmpuleFormica 7 Special Order Ampule

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 4 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
48951-414748951-4147-1

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 3 matching rows.

Name, UNII, Kind table
NameUNIIKind
FORMICA RUFA55H0W83JO5ACTIB
WATER059QF0KO0RIACT
SODIUM CHLORIDE451W47IQ8XIACT

Source Document#

Source XML

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
c4e45f10-398f-8a4a-e053-2995a90a64c170965daa-4de6-dd17-e053-2a91aa0a03e12021-06-16WarningsExact identifier
spl set id: 70965daa-4de6-dd17-e053-2a91aa0a03e1

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.