FDA.reportPublic FDA data

FERRIC HEMOGLOBIN CHLORIDE

Manufacturer
Guangzhou Natural Health Technology Co., Ltd
Effective date
2024-08-04
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-01 20:57:12

Label at a glance#

ProductFERRIC HEMOGLOBIN CHLORIDE
Active ingredientSILICON DIOXIDE, TITANIUM DIOXIDE
Label structure10 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Silicon dioxide is 0.1%

Titanium dioxide 0.45%

OTC - PURPOSE SECTION

Nourish blood and qi

Nourish blood and qi

INDICATIONS & USAGE SECTION

Promote bone growth

WARNINGS SECTION

For external use only.

Keep away from fire and flame

OTC - WHEN USING SECTION

WHEN USING THIS PRODUCT

·Store in a sealed, room temperature dry place

OTC - STOP USE SECTION

STOP USE AND ASK A DOCTOR

IF DISCOMFORT PER SISTS

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

KEEP OUT OF REACH OF CHILDREN

NOT SUITABLE FOR PEOPLE UNDER 3 YEARS OLD

DOSAGE & ADMINISTRATION SECTION

DIRECTIONS

ONCE A DAY, TAKE ONE TABLET EACH TIME. METHOD OF

CONSUMPTION: ORAL ADMINISTRATION RECORD NUMBER FO0D AND HEALTHG202444001188

INACTIVE INGREDIENT SECTION

SORBITOL, LACTOSE, MAGNESIUM STEARATE, CITRIC ACID, SILICA, SUCRALOSE, MENTHOL, VITAMIN C, COATING PREMIX (HYDROXYPROPYL METHYLCELLULOSE, POLYVINYLPYRROLIDONE K30, POLYETHYLENE GLYCOL, CARMINE ALUMINUM LAKE, INDIGO ALUMINUM LAKE, TALC POWDER, TITANIUM DIOXIDE, ERYTHRITE ALUMINUM LAKE, SEDUCTION RED ALUMINUM LAKE)

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

84634-002-0184634-002-01

Products#

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

DailyMed product names page 1 of 1 · 16 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
84634-00284634-002-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 15 matching rows.

Name, UNII, Kind table
NameUNIIKind
MAGNESIUM STEARATE70097M6I30IACT
POLYETHYLENE GLYCOL, UNSPECIFIED3WJQ0SDW1AIACT
ASCORBIC ACIDPQ6CK8PD0RIACT
TALC7SEV7J4R1UIACT
FD&C RED NO. 40 ALUMINUM LAKE6T47AS764TIACT
POVIDONE K30U725QWY32XIACT
SILICON DIOXIDEETJ7Z6XBU4ACTIB
TITANIUM DIOXIDE15FIX9V2JPACTIB
SUCRALOSE96K6UQ3ZD4IACT
SORBITOL506T60A25RIACT
CITRIC ACID MONOHYDRATE2968PHW8QPIACT
LACTOSE, UNSPECIFIED FORMJ2B2A4N98GIACT
MENTHOLL7T10EIP3AIACT
HYPROMELLOSES3NXW29V3WOIACT
ALUMINUM OXIDELMI26O6933IACT

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
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
1fc4322d-720f-0299-e063-6294a90ac5a61f00a9d4-bb4f-6a6f-e063-6394a90a99382024-08-15WarningsExact identifier
spl set id: 1f00a9d4-bb4f-6a6f-e063-6394a90a9938

Reported adverse events (FAERS/openFDA)#

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