FDA.reportPublic FDA data

Formica Stibium comp. Special Order

Product NDC
48951-4102
11-digit product format
489514102
Labeler code
48951
Product ID
48951-4102_6ac1cba3-ea3b-0d77-e053-2a91aa0a247c
Type
HUMAN OTC DRUG
Nonproprietary name
Formica Stibium comp. Special Order
Dosage form
LIQUID
Route
ORAL
Labeler
Uriel Pharmacy Inc.
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
2009-09-01
Marketing end
0000-00-00
Substance
SUS SCROFA LUNG; ANTIMONY; SILICON DIOXIDE; FORMICA RUFA
Active strength
6 [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL
NDC exclude flag
No
Listing certified through
2020-12-31
Current FDA listing
Historical FDA.report record

NDC auxiliary status#

These records are reproduced from FDA’s unfinished, excluded, and compounder listings. They describe what appeared in the source files; a missing record does not establish a regulatory status. View all current auxiliary records, including entries without an NDC. · View the auxiliary file history.

Current NDC status page 1 of 1 · 2 matching rows.

Dataset, Scope, Product NDC table
DatasetScopeProduct NDCPackage NDCCodeStatusReporting periodSource date
excluded productproduct48951-4102DDiscontinued by firm2026-10-05
excluded packagepackage48951-410248951-4102-3DDiscontinued by firm2026-10-05

Observed NDC auxiliary status history#

This history shows the information present in each captured FDA auxiliary file. It is not a continuous regulatory timeline, and a missing record does not establish a status.

Historic NDC status page 1 of 1 · 2 matching rows.

View current auxiliary records. · View the auxiliary file history.

Captured / source date, Dataset, Scope table
Captured / source dateDatasetScopeProduct NDCPackage NDCCodeStatusReporting periodArchiveSnapshotSource SHA-256
2025-12-14 17:58 UTC · source 2025-12-05excluded productproduct48951-4102DDiscontinued by firmexcluded / ndc_excluded.zipd630ba8d3edf…732f749b63fb…
2025-12-14 17:58 UTC · source 2025-12-05excluded packagepackage48951-410248951-4102-3DDiscontinued by firmexcluded / ndc_excluded.zipd630ba8d3edf…732f749b63fb…

Reported adverse events (FAERS/openFDA)#

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

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
ANTIMONYACTIVE INGREDIENT9IT35J3UV3FORMICA STIBIUM COMP. SPECIAL ORDER LIQUID [URIEL PHARMACY INC.]1
COLLOIDAL SILICON DIOXIDEACTIVE INGREDIENTETJ7Z6XBU4FORMICA STIBIUM COMP. SPECIAL ORDER LIQUID [URIEL PHARMACY INC.]1
FORMICA RUFAACTIVE INGREDIENT55H0W83JO5FORMICA STIBIUM COMP. SPECIAL ORDER LIQUID [URIEL PHARMACY INC.]1
SUS SCROFA LUNGACTIVE INGREDIENT7GL3G1COB3FORMICA STIBIUM COMP. SPECIAL ORDER LIQUID [URIEL PHARMACY INC.]1
ANTIMONYACTIVE MOIETY9IT35J3UV3FORMICA STIBIUM COMP. SPECIAL ORDER LIQUID [URIEL PHARMACY INC.]1
COLLOIDAL SILICON DIOXIDEACTIVE MOIETYETJ7Z6XBU4FORMICA STIBIUM COMP. SPECIAL ORDER LIQUID [URIEL PHARMACY INC.]1
FORMICA RUFAACTIVE MOIETY55H0W83JO5FORMICA STIBIUM COMP. SPECIAL ORDER LIQUID [URIEL PHARMACY INC.]1
SUS SCROFA LUNGACTIVE MOIETY7GL3G1COB3FORMICA STIBIUM COMP. SPECIAL ORDER LIQUID [URIEL PHARMACY INC.]1
WATERINACTIVE INGREDIENT059QF0KO0RFORMICA STIBIUM COMP. SPECIAL ORDER LIQUID [URIEL PHARMACY INC.]1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
48951-4102FORMICA STIBIUM COMP. SPECIAL ORDER LIQUID [URIEL PHARMACY INC.]2Legacy NDC20180501_439073f2-1dee-4b4e-a65e-74aee1c73c2b.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
48951-4102-34895141020360 mL in 1 BOTTLE, DROPPER (48951-4102-3) 60 ml2009-09-010000-00-00NoNoCurrent