NDC 43074-207-01 - VenomX

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
43074-207
Requested NDC
43074-207-01
Package NDCs from labels
43074-207-01, 43074-207-02
Manufacturer
Phillips Company
Effective date
2010-09-04
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
VenomX - Phillips CompanyPhillips Company2010-09-04HUMAN OTC DRUG LABEL

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
43074-207-022019-11-13C16284748780-197449f38-c533-f6ea-e053-dbdaa90aa703DRUG FACTS

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
43074-207-01VenomX3 mL in 1 BOTTLE, DROPPERLIQUID313
43074-207-02VenomX1 in 1 BOTTLE, PLASTICLIQUID113

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
43074-207VENOMX (ZINC ACETATE) LIQUID [PHILLIPS COMPANY]13Legacy NDC, 2 package rows20120517_1cfba647-929e-4525-b37a-b912a5a0ec4f.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
zinc acetateACTIVE INGREDIENTFM5526K07AVENOMX (ZINC ACETATE) LIQUID [PHILLIPS COMPANY]13
zincACTIVE MOIETYJ41CSQ7QDSVENOMX (ZINC ACETATE) LIQUID [PHILLIPS COMPANY]13
ascorbic acidINACTIVE INGREDIENTPQ6CK8PD0RVENOMX (ZINC ACETATE) LIQUID [PHILLIPS COMPANY]13
calcium gluconateINACTIVE INGREDIENTSQE6VB453KVENOMX (ZINC ACETATE) LIQUID [PHILLIPS COMPANY]13
chlorhexidine gluconateINACTIVE INGREDIENTMOR84MUD8EVENOMX (ZINC ACETATE) LIQUID [PHILLIPS COMPANY]13
dimethyl sulfoxideINACTIVE INGREDIENTYOW8V9698HVENOMX (ZINC ACETATE) LIQUID [PHILLIPS COMPANY]13
dipropylene glycolINACTIVE INGREDIENTE107L85C40VENOMX (ZINC ACETATE) LIQUID [PHILLIPS COMPANY]13
glycerinINACTIVE INGREDIENTPDC6A3C0OXVENOMX (ZINC ACETATE) LIQUID [PHILLIPS COMPANY]13
magnesium stearateINACTIVE INGREDIENT70097M6I30VENOMX (ZINC ACETATE) LIQUID [PHILLIPS COMPANY]13
methylparabenINACTIVE INGREDIENTA2I8C7HI9TVENOMX (ZINC ACETATE) LIQUID [PHILLIPS COMPANY]13
sodium dodecylbenzenesulfonateINACTIVE INGREDIENT554127163YVENOMX (ZINC ACETATE) LIQUID [PHILLIPS COMPANY]13
sodium hydroxideINACTIVE INGREDIENT55X04QC32IVENOMX (ZINC ACETATE) LIQUID [PHILLIPS COMPANY]13
sorbic acidINACTIVE INGREDIENTX045WJ989BVENOMX (ZINC ACETATE) LIQUID [PHILLIPS COMPANY]13
stearic acidINACTIVE INGREDIENT4ELV7Z65APVENOMX (ZINC ACETATE) LIQUID [PHILLIPS COMPANY]13
waterINACTIVE INGREDIENT059QF0KO0RVENOMX (ZINC ACETATE) LIQUID [PHILLIPS COMPANY]13
witch hazelINACTIVE INGREDIENT101I4J0U34VENOMX (ZINC ACETATE) LIQUID [PHILLIPS COMPANY]13

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 22 of 52 · 1,033 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
ChloraPrep One-StepCHLORHEXIDINE GLUCONATE AND ISOPROPYL ALCOHOLCareFusion 213, LLC8529596f-37e4-c44e-e053-2a91aa0ad0142025-10-30WarningsExact identifier
unii: MOR84MUD8E
Diphenhydramine HCl and Zinc AcetateEXTRA STRENGTH ITCH RELIEFHEB2aedbf1d-c8b7-4d5d-83ee-e38872c37d4f2025-10-30WarningsExact identifier
unii: FM5526K07A
Extra Strength Itch ReliefDIPHENHYDRAMINE HCL AND ZINC ACETATEMeijer Distribution Inc02f9e270-6047-83b6-e063-6394a90afc272025-10-30WarningsExact identifier
unii: FM5526K07A
GlycerinGLYCERINChain Drug Marketing Association Inc.424d91f0-ecf9-6d9b-e063-6394a90a80062025-10-29WarningsExact identifier
unii: PDC6A3C0OX
ChloraPrep One-StepCHLORHEXIDINE GLUCONATE AND ISOPROPYL ALCOHOLCareFusion 213, LLC8578da30-a155-2505-e053-2991aa0a2c042025-10-29WarningsExact identifier
unii: MOR84MUD8E
hemorrhoidalGLYCERIN, PHENYLEPHRINE HCL, PRAMOXINE HCL, WHITE PETROLATUMPublix Super Markets Inc354a640c-bc7e-45c8-9df0-8b5b01767f5c2025-10-29WarningsExact identifier
unii: PDC6A3C0OX
Sterile WaterWATERICU Medical Inc.1c0bbcb7-5ed6-4ee7-b297-080d3359474e2025-10-29Boxed warning, Warnings, Adverse reactionsExact identifier
unii: 059QF0KO0R
Bacteriostatic WaterWATERHenry Schein, Inc.a833502e-a622-4e81-8c58-cef6ccb6c4c92025-10-27Boxed warning, Warnings, Adverse reactionsExact identifier
unii: 059QF0KO0R
LACRIFRESH HYDRAPFGLYCERIN, POVIDONEAVIZOR, S.A.41bbd23e-0ec8-eb18-e063-6294a90a46d12025-10-27WarningsExact identifier
unii: PDC6A3C0OX
LACRIFRESH HYDRAMAXPFGLYCERIN, POVIDONEAVIZOR, S.A.41be1604-89b4-7ec3-e063-6294a90a33312025-10-27WarningsExact identifier
unii: PDC6A3C0OX
GlycerinGLYCERINDSC Laboratories Inc.5e97aa5b-62e2-0664-e053-2a91aa0ac3412025-10-24WarningsExact identifier
unii: PDC6A3C0OX
GlycerinGLYCERINH E B3d03ce42-e671-6d76-e054-00144ff8d46c2025-10-24WarningsExact identifier
unii: PDC6A3C0OX
GlycerinGLYCERINChain Drug Consortium LLC022dd494-cb3c-4fa7-be99-4c38fabdc6122025-10-24WarningsExact identifier
unii: PDC6A3C0OX
GlycerinGLYCERINDSC Laboratories Inc.5e97c4d2-e41d-5bb6-e053-2a91aa0a31632025-10-24WarningsExact identifier
unii: PDC6A3C0OX
GlycerinGLYCERINCVS Pharmacy94e4a6f3-43d0-b2a5-e053-2a95a90aa1152025-10-24WarningsExact identifier
unii: PDC6A3C0OX
GlycerinGLYCERINChain Drug Marketing Association Inc.5e83d3ef-91c5-1c3a-e053-2a91aa0a93ed2025-10-24WarningsExact identifier
unii: PDC6A3C0OX
GlycerinGLYCERINRite Aid Corporation5da2ea79-f3bc-b82b-e053-2a91aa0af0af2025-10-24WarningsExact identifier
unii: PDC6A3C0OX
GlycerinGLYCERINRite Aid Corporation5da2ea79-f37a-b82b-e053-2a91aa0af0af2025-10-24WarningsExact identifier
unii: PDC6A3C0OX
GlycerinGLYCERINDSC Laboratories Inc.a381838b-d1ae-11c5-e053-2a95a90a7bcb2025-10-24WarningsExact identifier
unii: PDC6A3C0OX
GlycerinGLYCERINAmerisource Bergen/Good Neighbor Pharmacy90a4d385-d548-420b-91d2-54d5e819fcce2025-10-24WarningsExact identifier
unii: PDC6A3C0OX

Reported adverse events (FAERS/openFDA)#

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