NDC 48951-9072-01 - Viscum Crataegus

This NDC is not currently matched to an FDA NDC product listing in FDA.report, but it is a valid NDC-form code. FDA.report is showing the available DailyMed label context for the product root.

Product NDC
48951-9072
Requested NDC
48951-9072-01
Package NDCs from labels
48951-9072-1, 48951-9072-01
Manufacturer
Uriel Pharmacy Inc.
Effective date
2026-08-21
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
Viscum CrataegusUriel Pharmacy Inc.2026-08-21HUMAN OTC DRUG LABEL

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
48951-9072-1Viscum Crataegus10 in 1 BOXLIQUID103
48951-9072-1Viscum Crataegus1 mL in 1 AMPULELIQUID13

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
48951-9072VISCUM CRATAEGUS LIQUID [URIEL PHARMACY INC.]3Current NDC, Legacy NDC, 2 package rows20190612_64860e61-2938-4ac7-8072-da1a58946327.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
EQUISETUM ARVENSE TOPACTIVE INGREDIENT1DP6Y6B65ZVISCUM CRATAEGUS LIQUID [URIEL PHARMACY INC.]1
GOLDACTIVE INGREDIENT79Y1949PYOVISCUM CRATAEGUS LIQUID [URIEL PHARMACY INC.]1
HAWTHORN LEAF WITH FLOWERACTIVE INGREDIENT6OM09RPY36VISCUM CRATAEGUS LIQUID [URIEL PHARMACY INC.]1
VISCUM ALBUM FRUITING TOPACTIVE INGREDIENTBK9092J5MPVISCUM CRATAEGUS LIQUID [URIEL PHARMACY INC.]1
EQUISETUM ARVENSE TOPACTIVE MOIETY1DP6Y6B65ZVISCUM CRATAEGUS LIQUID [URIEL PHARMACY INC.]1
GOLDACTIVE MOIETY79Y1949PYOVISCUM CRATAEGUS LIQUID [URIEL PHARMACY INC.]1
HAWTHORN LEAF WITH FLOWERACTIVE MOIETY6OM09RPY36VISCUM CRATAEGUS LIQUID [URIEL PHARMACY INC.]1
VISCUM ALBUM FRUITING TOPACTIVE MOIETYBK9092J5MPVISCUM CRATAEGUS LIQUID [URIEL PHARMACY INC.]1
SODIUM CHLORIDEINACTIVE INGREDIENT451W47IQ8XVISCUM CRATAEGUS LIQUID [URIEL PHARMACY INC.]1
WATERINACTIVE INGREDIENT059QF0KO0RVISCUM CRATAEGUS LIQUID [URIEL PHARMACY INC.]1

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 68 of 68 · 1,350 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
ReHydrationADENOSINUM CYCLOPHOSPHORICUM, COFFEA CRUDA, GLANDULA SUPRARENALIS SUIS, HYPOTHALAMUS (BOVINE), KALI PHOSPHORICUM, NATRUM MURIATICUM, SARSAPARILLA, SILICEA, TARAXACUM OFFICINALE, THYROIDINUM (BOVINE)Energetix Corp9883c502-9782-451e-9eec-c54d7b054f312017-01-31WarningsExact identifier
unii: 451W47IQ8X
Estrogen and ProgesteroneAGNUS CASTUS, ANGELICA SINENSIS, APIS MELLIFICA, ARNICA MONTANA, CIMICIFUGA RACEMOSA, ESTRADIOL, ESTRIOL, FOLLICULINUM, GALIUM APARINE, GLYCYRRHIZA GLABRA, KOREAN GINSENG, OOPHORINUM (SUIS), PROGESTERONE, SEPIA, THUJA OCCIDENTALIS, VISCUM ALBUMProBLEN71fec93b-43b7-4ebb-ab5c-5f544d8e6cbf2017-01-12WarningsExact identifier
unii: BK9092J5MP
Tox-ChordALFALFA, ALUMINA, BENZOICUM ACIDUM, CARBONEUM, CETRARIA ISLANDICA, FOLLICULINUM, FUCUS VESICULOSUS, FUMARICUM ACIDUM, HEPAR SUIS, KALI CARBONICUM, KREOSOTUM, NATRUM MURIATICUM, PARAFFINUM, PETROLEUM, PHOSPHORICUM ACIDUM, PHOSPHORUS, PIX LIQUIDA, PLANTAGO MAJOR, PLUMBUM METALLICUM, PULSATILLA (VULGARIS), RADIUM BROMATUM, RESORCINUM, SALOL, SILICEA, SYMPHYTUM OFFICINALE, TABACUM, TEREBINTHINA, THYROIDINUM (BOVINE), TRITICUM REPENS, ZINCUM OXYDATUMEnergetix Corp6b0d1628-b20d-426e-9c84-5cceadca3f452016-11-11WarningsExact identifier
unii: 451W47IQ8X
Inflammation IIASTRAGALUS MEMBRANACEUS, ECHINACEA (ANGUSTIFOLIA), SARSAPARILLA (SMILAX REGELII), TABEBUIA IMPETIGINOSA, HYDRASTIS CANADENSIS, THYROIDINUM (SUIS), AURUM METALLICUM, CARBO ANIMALIS, CAUSTICUM, GELSEMIUM SEMPERVIRENS, NATRUM SULPHURICUM, PHOSPHORUS, SULPHUR, THUJA OCCIDENTALISBioActive Nutritional, Inc.4c36e714-f564-41d3-a6b8-60e633defaff2016-10-04WarningsExact identifier
unii: 79Y1949PYO
Sterile WaterWATERBaxter Healthcare Company210dc9ab-d6ca-4552-ac19-1be17792d2902016-05-31Warnings, Adverse reactionsExact identifier
unii: 059QF0KO0R
Sodium ChlorideSODIUM CHLORIDEBaxter Healthcare Corporation2a96096d-43cc-49b7-af53-b53c17f410012014-07-25Warnings, Adverse reactionsExact identifier
unii: 451W47IQ8X
SODIUM CHLORIDESODIUM CHLORIDEBaxter Healthcare Corporationb3b4b176-41f0-4ca8-90d4-3fba5707564a2014-02-21Exact identifier
unii: 451W47IQ8X
TIS-U-SOLSODIUM CHLORIDE, POTASSIUM CHLORIDE, MAGNESIUM SULFATE, SODIUM PHOSPHATE, AND POTASSIUM PHOSPHATEBaxter Healthcare Corporation9da4121f-d62d-4da4-8dfb-0494da16015f2014-02-21Exact identifier
unii: 451W47IQ8X
RingersSODIUM CHLORIDE, CALCIUM CHLORIDE, POTASSIUM CHLORIDE,Baxter Healthcare Corporatione1953d54-818d-46a6-8532-518ebae6d84e2012-06-13Exact identifier
unii: 451W47IQ8X
Lactated RingersSODIUM CHLORIDE, SODIUM LACTATE, POTASSIUM CHLORIDE, CALCIUM CHLORIDEBaxter Healthcare Corporationf09f80bf-2f8b-4420-865d-aec2d5e5cd4d2012-06-12Exact identifier
unii: 451W47IQ8X

Reported adverse events (FAERS/openFDA)#

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