Stibium 6

Product NDC: 48951-8213
11-digit product format: 489518213
Labeler code: 48951
Product ID: 48951-8213_4bad10f2-023f-985d-e063-6394a90a224d
Type: HUMAN OTC DRUG
Nonproprietary name: Stibium 6
Dosage form: LIQUID
Route: ORAL
Labeler: Uriel Pharmacy Inc.
Marketing category: UNAPPROVED HOMEOPATHIC
Marketing start: 2009-09-01
Substance: ANTIMONY
Active strength: 6 [hp_X]/mL
NDC exclude flag: No
Listing certified through: 2027-12-31
Current FDA listing: Yes

Additional Listing Data#

Finished product: Yes
Brand name base: Stibium 6
Listing expiration: 2027-12-31

Active Ingredients#

Ingredient, Strength table
Ingredient	Strength
ANTIMONY	6 [hp_X]/mL

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
Identifier	FDA.report destination
9IT35J3UV3	Internal UNII lookup

Harmonized SPL set identifiers#

SPL set identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
Identifier	FDA.report destination
b1188361-863f-46f6-9b02-3581b5e6687e	Available on FDA.report

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
48951-8213-1	2026-01-29	C162847	48780-1	49896155-a8cd-586f-e063-e6dba90add90	Stibium 6

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
48951-8213-1	Stibium 6	10 in 1 BOX	LIQUID	10		5
48951-8213-1	Stibium 6	1 mL in 1 AMPULE	LIQUID	1		5

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
Ingredient	Type	UNII	DailyMed label	SPL version
ANTIMONY	ACTIVE INGREDIENT	9IT35J3UV3	STIBIUM 6 LIQUID [URIEL PHARMACY INC.]	1
ANTIMONY	ACTIVE MOIETY	9IT35J3UV3	STIBIUM 6 LIQUID [URIEL PHARMACY INC.]	1
LACTOSE	INACTIVE INGREDIENT	J2B2A4N98G	STIBIUM 6 LIQUID [URIEL PHARMACY INC.]	1
SODIUM CHLORIDE	INACTIVE INGREDIENT	451W47IQ8X	STIBIUM 6 LIQUID [URIEL PHARMACY INC.]	1
WATER	INACTIVE INGREDIENT	059QF0KO0R	STIBIUM 6 LIQUID [URIEL PHARMACY INC.]	1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
48951-8213	STIBIUM 6 LIQUID [URIEL PHARMACY INC.]	4	Current NDC, Legacy NDC, 2 package rows	20241108_b1188361-863f-46f6-9b02-3581b5e6687e.zip

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
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Stibium 6	STIBIUM 6	Uriel Pharmacy Inc.	b1188361-863f-46f6-9b02-3581b5e6687e	2026-02-25	Warnings	Exact identifier ndc (product): 48951-8213

UNII, Preferred term, Registry number table
UNII	Preferred term	Registry number	Matched term
9IT35J3UV3	ANTIMONY	7440-36-0	ANTIMONY

Packages#

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Units	Marketing start	Marketing end	Sample	Exclude flag	Status
48951-8213-1	48951821301	10 AMPULE in 1 BOX (48951-8213-1) / 1 mL in 1 AMPULE	10 ampule	2009-09-01	0000-00-00	No	No	Current