LOA NEW-FREEDOM S

Manufacturer: CO LTD JUNG MIN
Effective date: 2021-04-24
Label type: HUMAN OTC DRUG LABEL
Version: 1
Source: full-release
Hydrated at: 2026-05-31 23:39:56

Label at a glance#

ProductLOA NEW-FREEDOM S

Active ingredientSULFATE ION

Label structure8 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

sulfate

INACTIVE INGREDIENT SECTION

sulfate

OTC - PURPOSE SECTION

anti oxident, anti inflammatory

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

KEEP OUT OF REACH OF THE CHILDREN

INDICATIONS & USAGE SECTION

take one capsule two times per day with water

WARNINGS SECTION

store in a cool dry place

DOSAGE & ADMINISTRATION SECTION

for oral use only

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

label

DailyMed Pharmacologic Classes#

Class, Version, Type table
Class	Version	Type	Effective
SULFATE ION Pharmacologic Class Indexing	2	Indexing - Pharmacologic Class	20180813

DailyMed Product Concepts#

Product concept, Relation, Version table
Product concept	Relation	Version	Effective
95250459-30e4-45c1-b08a-993044f49109	Product name	2	20250805
26acd337-b838-40ac-bcbc-05c3b81c8712	Product name	1	20170323

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
81841-0001-1	2022-07-29	C162847	48780-1	e4f33bdf-b0c9-d8a0-e053-dadaa90a6e4e	Drug Facts

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
81841-0001-1	LOA NEW-FREEDOM S	60 in 1 BOTTLE	CAPSULE	60		1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
81841-0001	LOA NEW-FREEDOM S (SULFATE) CAPSULE [CO LTD JUNG MIN]	1	Legacy NDC, 1 package rows	20210426_c0c15088-0ef2-97a2-e053-2995a90a1cb0.zip

Products#

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

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

LOA NEW-FREEDOM S
sulfate
WATER
SULFATE ION

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
81841-0001	81841-0001-1

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 2 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
WATER	059QF0KO0R	IACT
SULFATE ION	7IS9N8KPMG	ACTIB

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
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
c0c150a1-24fc-eb01-e053-2a95a90af14b			c0c15088-0ef2-97a2-e053-2995a90a1cb0	2021-04-24	Warnings	Exact identifier spl id: c0c150a1-24fc-eb01-e053-2a95a90af14b spl set id: c0c15088-0ef2-97a2-e053-2995a90a1cb0

Reported adverse events (FAERS/openFDA)#

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