Placenta Compositum 2.2 ml Injection

Manufacturer
Heel Inc
Effective date
2012-05-14
Label type
HUMAN PRESCRIPTION DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 02:03:46

Label at a glance#

ProductPlacenta Compositum
Active ingredientHORSE CHESTNUT, LACTIC ACID, L-, CLAVICEPS PURPUREA SCLEROTIUM, CUPRIC SULFATE, MELILOTUS OFFICINALIS TOP, SUS SCROFA PLACENTA, SOLANUM NIGRUM WHOLE, STROPHANTHUS HISPIDUS SEED, SUS SCROFA EMBRYO, SODIUM PYRUVATE, SUS SCROFA VEIN, SUS SCROFA ARTERY, SUS SCROFA UMBILICAL CORD, TOBACCO LEAF, VIPERA BERUS VENOM, BARIUM CARBONATE, LEAD IODIDE
Label structure5 sections

Dosage and administration

The dosage schedules listed below can be used as a general guide for the administration of Placenta compositum Injection Solution. Placenta compositum Injection Solution shows individual differences in clinical response. Therefore, the dosage for each patient should be individualized according to the patient’s response to therapy. Adults and children 7 years and older: in acute disorders, 1 ampule per day, otherwi...

Label contents#

Full prescribing information#

DESCRIPTION

DESCRIPTION SECTION

Injection Solution Ingredient Information: Each 2.2 ml ampule contains: Aesculus hippocastanum 4X, Sarcolacticum acidum 4X, Secale cornutum 4X, Cuprum sulphuricum 6X, Melilotus officinalis 6X, Placenta suis 6X, Solanum nigrum 6X, Strophanthus hispidus 6X, Embryo suis 8X, Natrum pyruvicum 8X, Vena suis 8X, Arteria suis 10X, Funiculus umbilicalis suis 10X, Tabacum 10X, Vipera berus 10X, Baryta carbonica 13X, Plumbum iodatum 18X 22 mcl each. Inactive ingredient: Sterile isotonic sodium chloride
solution

INDICATION AND USAGE

INDICATIONS & USAGE SECTION

Placenta compositum Injection Solution is indicated for stimulation of metabolic functions of the peripheral circulation of the blood as well as for a revitalizing and stimulating effect on the liver and peripheral vascular system.

Placenta compositum Injection Solution is classified as a homeopathic combination drug.

Botanical ingredients:
    Aesculus hippocastanum (horse chestnut)
    Melilotus officinalis (yellow sweet clover)
    Secale cornutum (rye ergot)
    Solanum nigrum (black nightshade)
    Strophanthus hispidus (Strophanthus)
    Tabacum (tobacco)

Mineral ingredients:
    Baryta carbonica (barium carbonate)
    Cuprum sulphuricum (copper sulfate)
    Natrum pyruvicum (sodium pyruvate)
    Plumbum iodatum (lead iodide)
    Sarcolacticum acidum (L-lactic acid)

Animal-derived ingredients
    Arteria suis (porcine artery)
    Embryo suis (porcine embryo)
    Funiculus umbilicalis suis (porcine umbilical cord)
    Placenta suis (porcine placenta)
    Vena suis (porcine vein)
    Vipera berus (common viper)




DOSAGE AND ADMINISTRATION

DOSAGE & ADMINISTRATION SECTION

The dosage schedules listed below can be used as a general guide for the administration of Placenta compositum Injection Solution. Placenta compositum Injection Solution shows individual differences in clinical response. Therefore, the dosage for each patient should be individualized according to the patient’s response to therapy.

Adults and children 7 years and older: in acute disorders, 1 ampule per day, otherwise 1 ampule, 1 to 3 times per week IM/SC/IV/ID. Children ages 2 to 6 receive ½ the adult dosage.

Discard unused solution.


WARNINGS

WARNINGS SECTION

Warnings and Precautions
If pain persists or worsens, if new symptoms occur, or if redness or swelling is present, the patient should be carefully re-evaluated because these could be signs of a serious condition.

Pregnancy Category C. Animal reproduction studies have not been conducted with this drug. It is also not known whether this drug can cause fetal harm when administered to a pregnant woman or can affect reproduction capacity. This drug should be given to a pregnant woman only if clearly needed.

To report SUSPECTED ADVERSE REACTIONS, contact Heel Inc. at 1.800.920.9203 or info@heelusa.com or FDA at 1-800-FDA-1088 or www.fda.gov/medwatch

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Placenta Compositum Injection.jpg
Placenta Compositum Injection.jpg



DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
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6bd95106-a412-1dad-b9cc-4cb74bfb27ceProduct name220230315
0306390c-dd77-4363-afe0-63c58088b2a1Product name120220120
503ea967-4b9c-48cf-9e87-c7975295849dProduct name220220120
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419aab54-5d5a-4146-9453-026d4a9991beProduct name220170525
26acd337-b838-40ac-bcbc-05c3b81c8712Product name120170323
08ffbcbf-26df-b99c-1dab-64fc4cfae89fProduct name220160823
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ed912195-5da0-0f2f-6f4b-3ef17710cbe3Product name120140508

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
50114-7055-12019-11-13C16284748780-197449f38-c1bb-f6ea-e053-dbdaa90aa703Placenta Compositum 2.2 ml Injection

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
50114-7055-1Placenta Compositum10 in 1 CARTONINJECTION101
50114-7055-1Placenta Compositum2.2 mL in 1 VIALINJECTION2.21

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
50114-7055PLACENTA COMPOSITUM (HORSE CHESTNUT AND LACTIC ACID, L- AND CLAVICEPS PURPUREA SCLEROTIUM AND CUPRIC SULFATE AND MELILOTUS OFFICINALIS TOP AND SUS SCROFA PLACENTA AND SOLANUM NIGRUM WHOLE AND STROPHANTHUS HISPIDUS SEED AND SUS SCROFA EMBRYO AND SODIUM PYRUVATE AND SUS SCROFA VEIN AND SUS SCROFA ARTERY AND SUS SCROFA UMBILICAL CORD AND TOBACCO LEAF AND VIPERA BERUS VENOM AND BARIUM CARBONATE AND LEAD IODIDE) INJECTION [HEEL INC]1Legacy NDC, 2 package rows20120514_481bd51c-afc6-4b33-abce-6f94ef6b1483.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
BARIUM CARBONATEACTIVE INGREDIENT6P669D8HQ81
CLAVICEPS PURPUREA SCLEROTIUMACTIVE INGREDIENT01G9XEA93N1
CUPRIC SULFATEACTIVE INGREDIENTLRX7AJ16DT1
HORSE CHESTNUTACTIVE INGREDIENT3C18L6RJAZ1
LACTIC ACID, L-ACTIVE INGREDIENTF9S9FFU82N1
LEAD IODIDEACTIVE INGREDIENTOTL90F2GLT1
MELILOTUS OFFICINALIS TOPACTIVE INGREDIENTGM6P02J2DX1
SODIUM PYRUVATEACTIVE INGREDIENTPOD38AIF081
SOLANUM NIGRUM WHOLEACTIVE INGREDIENT0FMD6WV47M1
STROPHANTHUS HISPIDUS SEEDACTIVE INGREDIENTMO892VI77K1
SUS SCROFA ARTERYACTIVE INGREDIENT63O327782Q1
SUS SCROFA EMBRYOACTIVE INGREDIENT9928MC12VO1
SUS SCROFA PLACENTAACTIVE INGREDIENTC8CV8867O81
SUS SCROFA UMBILICAL CORDACTIVE INGREDIENT118OYG6W3H1
SUS SCROFA VEINACTIVE INGREDIENT2510RH3I891
TOBACCO LEAFACTIVE INGREDIENT6YR2608RSU1
VIPERA BERUS VENOMACTIVE INGREDIENT0ORO6NCA4M1
CARBONATE IONACTIVE MOIETY7UJQ5OPE7D1
CLAVICEPS PURPUREA SCLEROTIUMACTIVE MOIETY01G9XEA93N1
HORSE CHESTNUTACTIVE MOIETY3C18L6RJAZ1
LACTIC ACID, L-ACTIVE MOIETYF9S9FFU82N1
LEAD IODIDEACTIVE MOIETYOTL90F2GLT1
MELILOTUS OFFICINALIS TOPACTIVE MOIETYGM6P02J2DX1
SODIUM CATIONACTIVE MOIETYLYR4M0NH371
SOLANUM NIGRUM WHOLEACTIVE MOIETY0FMD6WV47M1
STROPHANTHUS HISPIDUS SEEDACTIVE MOIETYMO892VI77K1
SULFATE IONACTIVE MOIETY7IS9N8KPMG1
SUS SCROFA ARTERYACTIVE MOIETY63O327782Q1
SUS SCROFA EMBRYOACTIVE MOIETY9928MC12VO1
SUS SCROFA PLACENTAACTIVE MOIETYC8CV8867O81
SUS SCROFA UMBILICAL CORDACTIVE MOIETY118OYG6W3H1
SUS SCROFA VEINACTIVE MOIETY2510RH3I891
TOBACCO LEAFACTIVE MOIETY6YR2608RSU1
VIPERA BERUS VENOMACTIVE MOIETY0ORO6NCA4M1
SODIUM CHLORIDEINACTIVE INGREDIENT451W47IQ8X1

Products#

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

DailyMed product names page 1 of 1 · 25 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
50114-705550114-7055-1

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 18 matching rows.

Source Document#

Source XML

Inactive ingredient matches#

Inactive Ingredient Database values describe FDA-listed use contexts. The match method and ambiguity count are shown because ingredient names, routes, and dosage forms are not always unique. Browse recovered IID releases and source provenance.

Inactive ingredient links page 1 of 3 · 134 matching rows.

DailyMed ingredient, IID ingredient, UNII table
DailyMed ingredientIID ingredientUNIIDosage form / routePotencyMaximum daily exposureMatch
SODIUM CHLORIDESODIUM CHLORIDE451W47IQ8XINJECTION / INTRABURSAL9 mgExact identifier — unii candidate
134 equally ranked IID candidates
SODIUM CHLORIDESODIUM CHLORIDE451W47IQ8XINJECTION, SOLUTION / PARENTERAL210 mgExact identifier — unii candidate
134 equally ranked IID candidates
SODIUM CHLORIDESODIUM CHLORIDE451W47IQ8XIMPLANT / SUBCUTANEOUS77 mgExact identifier — unii candidate
134 equally ranked IID candidates
SODIUM CHLORIDESODIUM CHLORIDE451W47IQ8XSPRAY, METERED / NASAL36 mgExact identifier — unii candidate
134 equally ranked IID candidates
SODIUM CHLORIDESODIUM CHLORIDE451W47IQ8XINJECTION, POWDER, FOR SOLUTION / SUBCUTANEOUS0.68 %w/vExact identifier — unii candidate
134 equally ranked IID candidates
SODIUM CHLORIDESODIUM CHLORIDE451W47IQ8XGEL / OPHTHALMIC0.9 %w/vExact identifier — unii candidate
134 equally ranked IID candidates
SODIUM CHLORIDESODIUM CHLORIDE451W47IQ8XTABLET, CHEWABLE / ORAL20 mgExact identifier — unii candidate
134 equally ranked IID candidates
SODIUM CHLORIDESODIUM CHLORIDE451W47IQ8XSUSPENSION / RESPIRATORY (INHALATION)43 mgExact identifier — unii candidate
134 equally ranked IID candidates
SODIUM CHLORIDESODIUM CHLORIDE451W47IQ8XSUSPENSION / TOPICAL0.32 %w/vExact identifier — unii candidate
134 equally ranked IID candidates
SODIUM CHLORIDESODIUM CHLORIDE451W47IQ8XINJECTION, SUSPENSION / SOFT TISSUE26 mgExact identifier — unii candidate
134 equally ranked IID candidates
SODIUM CHLORIDESODIUM CHLORIDE451W47IQ8XTABLET, COATED / ORAL54.7 mgExact identifier — unii candidate
134 equally ranked IID candidates
SODIUM CHLORIDESODIUM CHLORIDE451W47IQ8XPOWDER / TOPICALNAExact identifier — unii candidate
134 equally ranked IID candidates
SODIUM CHLORIDESODIUM CHLORIDE451W47IQ8XINHALANT / RESPIRATORY (INHALATION)3 mgExact identifier — unii candidate
134 equally ranked IID candidates
SODIUM CHLORIDESODIUM CHLORIDE451W47IQ8XINJECTION, SOLUTION / SUBARACHNOID0.9 %w/vExact identifier — unii candidate
134 equally ranked IID candidates
SODIUM CHLORIDESODIUM CHLORIDE451W47IQ8XSOLUTION / TOPICAL210 mgExact identifier — unii candidate
134 equally ranked IID candidates
SODIUM CHLORIDESODIUM CHLORIDE451W47IQ8XINJECTION, SOLUTION / INTRACAUDAL210 mgExact identifier — unii candidate
134 equally ranked IID candidates
SODIUM CHLORIDESODIUM CHLORIDE451W47IQ8XINJECTION, POWDER, FOR SOLUTION / INTRAPLEURAL226 mgExact identifier — unii candidate
134 equally ranked IID candidates
SODIUM CHLORIDESODIUM CHLORIDE451W47IQ8XINJECTION, SUSPENSION, EXTENDED RELEASE / INTRAMUSCULAR24 mgExact identifier — unii candidate
134 equally ranked IID candidates
SODIUM CHLORIDESODIUM CHLORIDE451W47IQ8XINJECTION / INFILTRATION648 mgExact identifier — unii candidate
134 equally ranked IID candidates
SODIUM CHLORIDESODIUM CHLORIDE451W47IQ8XINJECTION, POWDER, FOR SOLUTION / INTRA-ARTERIAL1.35 mgExact identifier — unii candidate
134 equally ranked IID candidates
SODIUM CHLORIDESODIUM CHLORIDE451W47IQ8XSUSPENSION/ DROPS / AURICULAR (OTIC)3 mgExact identifier — unii candidate
134 equally ranked IID candidates
SODIUM CHLORIDESODIUM CHLORIDE451W47IQ8XINJECTION, SOLUTION, CONCENTRATE / INTRAOCULAR0.86 %w/vExact identifier — unii candidate
134 equally ranked IID candidates
SODIUM CHLORIDESODIUM CHLORIDE451W47IQ8XENEMA / RECTAL0.7 %w/wExact identifier — unii candidate
134 equally ranked IID candidates
SODIUM CHLORIDESODIUM CHLORIDE451W47IQ8XLIQUID / INTRAVENOUS6320 mgExact identifier — unii candidate
134 equally ranked IID candidates
SODIUM CHLORIDESODIUM CHLORIDE451W47IQ8XTABLET, FILM COATED / ORAL100 mgExact identifier — unii candidate
134 equally ranked IID candidates
SODIUM CHLORIDESODIUM CHLORIDE451W47IQ8XJELLY / NASALNAExact identifier — unii candidate
134 equally ranked IID candidates
SODIUM CHLORIDESODIUM CHLORIDE451W47IQ8XINJECTION, SUSPENSION, LIPOSOMAL / EPIDURAL11 mgExact identifier — unii candidate
134 equally ranked IID candidates
SODIUM CHLORIDESODIUM CHLORIDE451W47IQ8XCREAM / TOPICAL0.4 %w/wExact identifier — unii candidate
134 equally ranked IID candidates
SODIUM CHLORIDESODIUM CHLORIDE451W47IQ8XINJECTION, POWDER, FOR SOLUTION / INTRATHECAL1.35 mgExact identifier — unii candidate
134 equally ranked IID candidates
SODIUM CHLORIDESODIUM CHLORIDE451W47IQ8XINJECTION, SOLUTION / INTRATHECAL131 mgExact identifier — unii candidate
134 equally ranked IID candidates
SODIUM CHLORIDESODIUM CHLORIDE451W47IQ8XPOWDER, FOR SOLUTION / OPHTHALMIC0.9 %w/wExact identifier — unii candidate
134 equally ranked IID candidates
SODIUM CHLORIDESODIUM CHLORIDE451W47IQ8XINJECTION / INTRA-ARTERIAL278 mgExact identifier — unii candidate
134 equally ranked IID candidates
SODIUM CHLORIDESODIUM CHLORIDE451W47IQ8XINJECTION, POWDER, FOR SUSPENSION / INTRA-ARTICULAR45 mgExact identifier — unii candidate
134 equally ranked IID candidates
SODIUM CHLORIDESODIUM CHLORIDE451W47IQ8XINJECTION / INTRAVITREAL10 %w/vExact identifier — unii candidate
134 equally ranked IID candidates
SODIUM CHLORIDESODIUM CHLORIDE451W47IQ8XSOLUTION / INTRAPERITONEAL0.54 %w/vExact identifier — unii candidate
134 equally ranked IID candidates
SODIUM CHLORIDESODIUM CHLORIDE451W47IQ8XINJECTION, POWDER, FOR SOLUTION / INTRAMUSCULAR226 mgExact identifier — unii candidate
134 equally ranked IID candidates
SODIUM CHLORIDESODIUM CHLORIDE451W47IQ8XINJECTION / SUBCUTANEOUS1486 mgExact identifier — unii candidate
134 equally ranked IID candidates
SODIUM CHLORIDESODIUM CHLORIDE451W47IQ8XSUPPOSITORY / RECTAL140 mgExact identifier — unii candidate
134 equally ranked IID candidates
SODIUM CHLORIDESODIUM CHLORIDE451W47IQ8XPOWDER, FOR SUSPENSION / ORAL98 mgExact identifier — unii candidate
134 equally ranked IID candidates
SODIUM CHLORIDESODIUM CHLORIDE451W47IQ8XINJECTION / DENTAL0.4 %w/vExact identifier — unii candidate
134 equally ranked IID candidates
SODIUM CHLORIDESODIUM CHLORIDE451W47IQ8XSUSPENSION / INTRAMUSCULAR9 mgExact identifier — unii candidate
134 equally ranked IID candidates
SODIUM CHLORIDESODIUM CHLORIDE451W47IQ8XINJECTION / INTRASYNOVIAL0.9 %w/vExact identifier — unii candidate
134 equally ranked IID candidates
SODIUM CHLORIDESODIUM CHLORIDE451W47IQ8XSOLUTION/ DROPS / TOPICAL0.86 %w/vExact identifier — unii candidate
134 equally ranked IID candidates
SODIUM CHLORIDESODIUM CHLORIDE451W47IQ8XINJECTION, SOLUTION / INTRA-ARTERIAL278 mgExact identifier — unii candidate
134 equally ranked IID candidates
SODIUM CHLORIDESODIUM CHLORIDE451W47IQ8XINJECTION, POWDER, LYOPHILIZED, FOR SOLUTION / INTRAVENOUS1800 mgExact identifier — unii candidate
134 equally ranked IID candidates
SODIUM CHLORIDESODIUM CHLORIDE451W47IQ8XINJECTION / INTRAVASCULAR0.86 %w/vExact identifier — unii candidate
134 equally ranked IID candidates
SODIUM CHLORIDESODIUM CHLORIDE451W47IQ8XINJECTION / INTRAVENOUS28773 mgExact identifier — unii candidate
134 equally ranked IID candidates
SODIUM CHLORIDESODIUM CHLORIDE451W47IQ8XTABLET, EXTENDED RELEASE / ORAL335.1 mgExact identifier — unii candidate
134 equally ranked IID candidates
SODIUM CHLORIDESODIUM CHLORIDE451W47IQ8XSHAMPOO / TOPICAL150 mgExact identifier — unii candidate
134 equally ranked IID candidates
SODIUM CHLORIDESODIUM CHLORIDE451W47IQ8XCAPSULE / ORAL6 mgExact identifier — unii candidate
134 equally ranked IID candidates
SODIUM CHLORIDESODIUM CHLORIDE451W47IQ8XSOAP / TOPICAL1.26 %w/wExact identifier — unii candidate
134 equally ranked IID candidates
SODIUM CHLORIDESODIUM CHLORIDE451W47IQ8XINJECTION, POWDER, FOR SOLUTION / INTRAVENOUS2922 mgExact identifier — unii candidate
134 equally ranked IID candidates
SODIUM CHLORIDESODIUM CHLORIDE451W47IQ8XSYSTEM / IONTOPHORESIS3.1 mgExact identifier — unii candidate
134 equally ranked IID candidates
SODIUM CHLORIDESODIUM CHLORIDE451W47IQ8XSOLUTION / EPIDURAL0.9 %w/vExact identifier — unii candidate
134 equally ranked IID candidates
SODIUM CHLORIDESODIUM CHLORIDE451W47IQ8XSOLUTION / IONTOPHORESIS0.6 %w/vExact identifier — unii candidate
134 equally ranked IID candidates
SODIUM CHLORIDESODIUM CHLORIDE451W47IQ8XSOLUTION / INTRAOCULAR320 mgExact identifier — unii candidate
134 equally ranked IID candidates
SODIUM CHLORIDESODIUM CHLORIDE451W47IQ8XSYSTEM / TOPICAL3.1 mgExact identifier — unii candidate
134 equally ranked IID candidates
SODIUM CHLORIDESODIUM CHLORIDE451W47IQ8XGEL / VAGINAL10 %w/wExact identifier — unii candidate
134 equally ranked IID candidates
SODIUM CHLORIDESODIUM CHLORIDE451W47IQ8XCAPSULE, EXTENDED RELEASE / ORAL41 mgExact identifier — unii candidate
134 equally ranked IID candidates
SODIUM CHLORIDESODIUM CHLORIDE451W47IQ8XINJECTION, POWDER, FOR SOLUTION / INTRAPERITONEAL226 mgExact identifier — unii candidate
134 equally ranked IID candidates

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
cc3f0e8b-fc8c-4a62-b3e7-d70b061977e4481bd51c-afc6-4b33-abce-6f94ef6b14832012-05-14WarningsExact identifier
spl id: cc3f0e8b-fc8c-4a62-b3e7-d70b061977e4
spl set id: 481bd51c-afc6-4b33-abce-6f94ef6b1483

Reported adverse events (FAERS/openFDA)#

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