Kali phos. Aurum

Product NDC: 48951-6011
Requested package NDC: 48951-6011-4
11-digit product format: 489516011
Labeler code: 48951
Product ID: 48951-6011_7cb0c15d-ee97-4d78-e053-2a91aa0aea1c
Type: HUMAN OTC DRUG
Nonproprietary name: Kali phos. Aurum
Dosage form: TABLET
Route: ORAL
Labeler: Uriel Pharmacy Inc.
Marketing category: UNAPPROVED HOMEOPATHIC
Marketing start: 2009-09-01
Marketing end: 0000-00-00
Substance: SILICON DIOXIDE; POTASSIUM PHOSPHATE, MONOBASIC; GOLD; FERROUS SULFATE
Active strength: 5 [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1
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 · 1 matching rows.

Dataset, Scope, Product NDC table
Dataset	Scope	Product NDC	Package NDC	Code	Status	Reporting period	Source date
excluded package	package	48951-6011	48951-6011-4	I	Inactivated by FDA		2026-10-15

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 · 9 matching rows.

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

Captured / source date, Code, Status table
Captured / source date	Code	Status	Snapshot	Source SHA-256
2025-12-14 17:58 UTC · source 2025-12-05	I	Inactivated by FDA	`d630ba8d3edf…`	`732f749b63fb…`
2025-08-27 00:01 UTC · source 2025-08-26	I	Inactivated by FDA	`f5e01cc5f278…`	`a2eaf40c39c3…`
2025-04-01 02:39 UTC · source 2025-03-31	I	Inactivated by FDA	`2ef7874e63bc…`	`57b86245f4fa…`
2025-03-28 20:22 UTC · source 2025-03-28	I	Inactivated by FDA	`a1b67e2a42f9…`	`c4cf2c586c0d…`
2025-03-22 03:12 UTC · source 2025-03-21	I	Inactivated by FDA	`cfe11265f3b6…`	`090c488252e2…`
2025-03-10 12:48 UTC · source 2025-03-10	I	Inactivated by FDA	`cdf11ea48f46…`	`ba0047e9e063…`
2025-02-02 03:52 UTC · source 2025-01-31	U	Excluded because listing certification expired	`302b2466d912…`	`e7b80fea0513…`
2025-01-20 13:05 UTC · source 2025-01-20	U	Excluded because listing certification expired	`ed331223b511…`	`672a5bd82f5f…`
2025-01-11 03:41 UTC · source 2025-01-10	U	Excluded because listing certification expired	`0efc9e666f02…`	`f202fb6c5f17…`

Reported adverse events (FAERS/openFDA)#

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

DailyMed Product Concepts#

Product concept, Relation, Version table
Product concept	Relation	Version	Effective
efd58dcf-540a-4531-8766-e713129ca6f2	Product name	1	20250307
4b7700e3-6e0e-45e5-9d22-6f754d61386e	Product name	2	20250304
726062af-1135-4707-a1d7-57256991bbf9	Product name	2	20250226
7cda52fc-125f-421c-8fea-bc1974370c49	Product name	2	20180703
0ca1d589-929b-4b33-bc5b-1d84abdafa6a	Product name	1	20150324
fc363c46-397b-4476-ac0f-70e43e8e4592	Product name	1	20150324
19c71a3d-ed9c-166b-a7e5-38c250c35631	Product name	1	20140508

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
48951-6011-4	2025-01-30	C162847	48780-1	2cef2736-8169-d83d-e063-dadaa90ab31f	Kali phos. Aurum

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
48951-6011-4	Kali phos. Aurum	250 in 1 BOTTLE, GLASS	TABLET	250		3

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
Ingredient	Type	UNII	DailyMed label	SPL version
COLLOIDAL SILICON DIOXIDE	ACTIVE INGREDIENT	ETJ7Z6XBU4	KALI PHOS. AURUM TABLET [URIEL PHARMACY INC.]	1
FERROUS SULFATE	ACTIVE INGREDIENT	39R4TAN1VT	KALI PHOS. AURUM TABLET [URIEL PHARMACY INC.]	1
GOLD	ACTIVE INGREDIENT	79Y1949PYO	KALI PHOS. AURUM TABLET [URIEL PHARMACY INC.]	1
POTASSIUM PHOSPHATE, MONOBASIC	ACTIVE INGREDIENT	4J9FJ0HL51	KALI PHOS. AURUM TABLET [URIEL PHARMACY INC.]	1
COLLOIDAL SILICON DIOXIDE	ACTIVE MOIETY	ETJ7Z6XBU4	KALI PHOS. AURUM TABLET [URIEL PHARMACY INC.]	1
FERROUS CATION	ACTIVE MOIETY	GW89581OWR	KALI PHOS. AURUM TABLET [URIEL PHARMACY INC.]	1
GOLD	ACTIVE MOIETY	79Y1949PYO	KALI PHOS. AURUM TABLET [URIEL PHARMACY INC.]	1
PHOSPHATE ION	ACTIVE MOIETY	NK08V8K8HR	KALI PHOS. AURUM TABLET [URIEL PHARMACY INC.]	1
LACTOSE	INACTIVE INGREDIENT	J2B2A4N98G	KALI PHOS. AURUM TABLET [URIEL PHARMACY INC.]	1
MAGNESIUM STEARATE	INACTIVE INGREDIENT	70097M6I30	KALI PHOS. AURUM TABLET [URIEL PHARMACY INC.]	1
STEARIC ACID	INACTIVE INGREDIENT	4ELV7Z65AP	KALI PHOS. AURUM TABLET [URIEL PHARMACY INC.]	1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
48951-6011	KALI PHOS. AURUM TABLET [URIEL PHARMACY INC.]	3	Legacy NDC, 1 package rows	20191018_02cff3a5-423e-4497-8b1f-90129a65ee46.zip

UNII, Preferred term, Registry number table
UNII	Preferred term	Registry number	Matched term
ETJ7Z6XBU4	SILICON DIOXIDE	7631-86-9	SILICON DIOXIDE
4J9FJ0HL51	POTASSIUM PHOSPHATE, MONOBASIC	7778-77-0	POTASSIUM PHOSPHATE, MONOBASIC
79Y1949PYO	GOLD	7440-57-5	GOLD
39R4TAN1VT	FERROUS SULFATE	7782-63-0	FERROUS SULFATE

Packages#

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Units	Marketing start	Marketing end	Sample	Exclude flag	Status
48951-6011-4	48951601104	250 TABLET in 1 BOTTLE, GLASS (48951-6011-4)	250 tablet	2009-09-01	0000-00-00	No	No	Current