Ferrum Phos

Product NDC: 44911-0042
Requested package NDC: 44911-0042-1
11-digit product format: 449110042
Labeler code: 44911
Product ID: 44911-0042_02669d53-7262-4f46-af13-7fd6651d908d
Type: HUMAN OTC DRUG
Nonproprietary name: Ferrum Phosphoricum
Dosage form: LIQUID
Route: ORAL
Labeler: Energique, Inc.
Marketing category: UNAPPROVED HOMEOPATHIC
Marketing start: 2012-10-02
Marketing end: 0000-00-00
Substance: FERRUM PHOSPHORICUM
Active strength: 30 [hp_C]/mL
NDC exclude flag: No
Listing certified through: 2021-12-31
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	44911-0042	44911-0042-1	D	Discontinued by firm		2026-10-16

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 · 11 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	D	Discontinued by firm	`d630ba8d3edf…`	`732f749b63fb…`
2025-08-27 00:01 UTC · source 2025-08-26	D	Discontinued by firm	`f5e01cc5f278…`	`a2eaf40c39c3…`
2024-10-04 04:10 UTC · source 2024-10-03	I	Inactivated by FDA	`367a005e9d99…`	`383a685ebd0f…`
2024-07-10 04:00 UTC · source 2024-07-09	I	Inactivated by FDA	`557ba5c1ecfa…`	`9c80585c8c6e…`
2024-05-28 21:12 UTC · source 2024-05-28	I	Inactivated by FDA	`8af77b9d5b6f…`	`d9bbb34c5368…`
2024-05-15 03:39 UTC · source 2024-05-14	I	Inactivated by FDA	`834df4deac94…`	`adcc014656a3…`
2024-03-11 06:39 UTC · source 2024-03-08	I	Inactivated by FDA	`1332a3947898…`	`d4bfe170f9cd…`
2022-08-30 03:57 UTC · source 2022-08-29	I	Inactivated by FDA	`fb8cb913e6d1…`	`eb8c232b6be0…`
2022-04-09 23:13 UTC · source 2022-04-08	I	Inactivated by FDA	`86f5da6cb304…`	`a595104c45d7…`
2022-04-04 05:40 UTC · source 2022-04-01	I	Inactivated by FDA	`bd6a592717d7…`	`303034d00443…`
2020-06-10 20:45 UTC · source 2020-06-10	I	Inactivated by FDA	`9bebd1f3094a…`	`5416666fcb17…`

Reported adverse events (FAERS/openFDA)#

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

FDA-Initiated Inactive NDC Indexing#

Effective, Related label table
Effective	Related label
2024-10-24	DRUG FACTS:
2022-01-28	DRUG FACTS:
2020-06-26	DRUG FACTS:
2020-01-31	DRUG FACTS:

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
Ingredient	Type	UNII	DailyMed label	SPL version
FERRUM PHOSPHORICUM	ACTIVE INGREDIENT	91GQH8I5F7	FERRUM PHOS (FERRUM PHOSPHORICUM) LIQUID [ENERGIQUE, INC.]	1
FERROSOFERRIC PHOSPHATE	ACTIVE MOIETY	91GQH8I5F7	FERRUM PHOS (FERRUM PHOSPHORICUM) LIQUID [ENERGIQUE, INC.]	1
ALCOHOL	INACTIVE INGREDIENT	3K9958V90M	FERRUM PHOS (FERRUM PHOSPHORICUM) LIQUID [ENERGIQUE, INC.]	1
WATER	INACTIVE INGREDIENT	059QF0KO0R	FERRUM PHOS (FERRUM PHOSPHORICUM) LIQUID [ENERGIQUE, INC.]	1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
44911-0042	FERRUM PHOS (FERRUM PHOSPHORICUM) LIQUID [ENERGIQUE, INC.]	4	Legacy NDC	20250521_f013a28c-4461-47a9-a230-01887bbf0a7f.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Units	Marketing start	Marketing end	Sample	Exclude flag	Status
44911-0042-1	44911004201	30 mL in 1 BOTTLE, DROPPER (44911-0042-1)	30 ml	2012-10-02	0000-00-00	No	No	Current