FUSION

Manufacturer
U.S. Pharmaceutical Corporation
Effective date
2023-11-10
Label type
DIETARY SUPPLEMENT
Version
4
Source
full-release
Hydrated at
2026-06-01 02:50:57

Label at a glance#

ProductFUSION
Active ingredientASCORBIC ACID, FERROUS FUMARATE, IRON POLYMALTOSE, LACTICASEIBACILLUS CASEI
Label structure6 sections

Label contents#

Full prescribing information#

STATEMENT OF IDENTITY SECTION

 Supplement Facts

 Serving Size: 1 Capsule



 Amount Per Serving


%DV* 
% Daily Value
for Pregnant or

Lactating Women

 Vitamin C 25 mg28% 21% 
 Iron
    (65 mg from Ferrous Fumarate)
    (65 mg from Polysaccharide Iron Complex)
130 mg 722% 481% 
 Lactobacillus casei (KE-99)
 200 Billion CFU/g**
30 mg † † 
 * %Daily Values are based on a 2,000 calorie intake for adults and children 12 years and older.       †  Daily value not established
 ** Colony Forming Units (CFU) per gram at time of manufacturing

Other Ingredients: Titanium Dioxide, FD&C Blue #1, FD&C Red # 40, Hypromellose, Microcrystalline Cellulose, Magnesium Stearate.

INDICATIONS: FusionTM is indicated for the treatment of iron deficiency anemia, which may occur due to an increased need for iron, a deficient intake of iron, or an excessive loss of iron. 

WARNINGS SECTION

WARNING: Accidental overdose of iron-containing products is a leading cause of fatal poisoning in children under 6. Keep this product out of reach of children. In case of accidental overdose, call a doctor or poison control center immediately.

HOW SUPPLIED: FusionTM are maroon opaque Vcaps® capsules printed in white with "US" Logo on the cap and "F" on the body. Packed in child resistant cap and light resistant bottle of 30 capsules (52747-0501-30). The listed product numbers are not National Drug Codes. Instead, US Pharmaceutical Corporation has assigned these product codes formatted according to standard industry practice to meet the formatting requirements of pharmacy and healthcare insurance computer systems.

You should contact your healthcare provider for medical advice about adverse events. To report a serious adverse event, contact US Pharmaceutical Corporation, P.O.Box 360465, Decatur, GA 30036.

DOSAGE & ADMINISTRATION SECTION

DOSAGE AND ADMINISTRATION: Adults (persons over 12 years of age), one (1) capsule daily, between meals, or as prescribed by a physician. Do not exceed recommended dosage. 

SAFE HANDLING WARNING SECTION

Store at room temperature 15° to 30°C (59° to 86°F) and dry place.

Vcaps® and the Vcaps® Logo are trademarks used under license.

Patent Numbers: Mexico MX/a/2008/004461; Singapore: 200802623-9 and other countries.

Rev. 08/2022

HEALTH CLAIM SECTION

Iron / Vitamin C / Probiotic Supplement Capsules

Packaging

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

FusioncapsFusioncaps

DailyMed Pharmacologic Classes#

Class, Version, Type table
ClassVersionTypeEffective
ASCORBIC ACID Pharmacologic Class Indexing2Indexing - Pharmacologic Class20180813
FERRIC CATION Pharmacologic Class Indexing3Indexing - Pharmacologic Class20180813

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
04cdd491-d111-4bc2-9549-75c575e1bd4bProduct name120200714
8390fb8b-6c75-416c-a9a1-70e8ed493b73Product name120200611
96a528e9-23e2-495f-81b9-ae87df2f7552Product name120191120
c5cd4727-ac49-4409-82b1-5bd8006c3ec7Product name120171122
3df56c93-5837-4523-aac2-4b1ec48b9676Product name220160719
a883b7cc-d320-41d7-92ae-c873457ae641Product name120151116
bb23e78e-9e64-4037-a1c1-0e1d8762700eProduct name120150325
ef06c001-572c-d95e-42f6-ee83da75673aProduct name120140508
fd21f957-6863-d07b-5a35-250186878716Product name120140508

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
52747-501-30FUSION30 in 1 BOTTLECAPSULE304

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
52747-501FUSION (VITAMIN C, FERROUS FUMARATE, POLYSACCHARIDE IRON COMPLEX, LACTOBACILLUS CASEI (KE-99)) CAPSULE [U.S. PHARMACEUTICAL CORPORATION]41 package rows20231205_216b32ae-335d-406e-a243-88aa6697a398.zip

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
52747-501-30EA - Each52747-501331d940e-eed6-4f5c-9311-9b91bd64fcd012016-01-13

Products#

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

DailyMed product names page 1 of 1 · 14 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
52747-50152747-501-30

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 10 matching rows.

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 · 4 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
Ascorbic AcidASCORBIC ACIDRenova Pharmaceuticals LLCa6481bae-2397-44c7-a51d-4f47ad91bd2c2026-08-19Warnings, Adverse reactionsName fallback
generic name: ASCORBIC ACID
AscorASCORBIC ACIDMcGuff Pharmaceuticals, Inc.388aad52-fc01-4784-9791-1dbc80c693062026-05-29Warnings, Adverse reactionsName fallback
generic name: ASCORBIC ACID
Ascorbic AcidASCORBIC ACIDFresenius Kabi USA, LLC1606e29f-0e80-4069-b688-daab9cbff20a2025-12-17Warnings, Adverse reactionsName fallback
generic name: ASCORBIC ACID
Skin Renewing SerumASCORBIC ACIDGuangzhou Danting Bath&Body Care Industry Co. Ltd396c2a8d-ac95-cbef-e063-6294a90aff392025-08-23WarningsName fallback
generic name: ASCORBIC ACID

Reported adverse events (FAERS/openFDA)#

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