NDC 84067-063 - Bee Venom Pain Cream

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
84067-063
Package NDCs from labels
84067-063-01
Manufacturer
Shantou Youjia E-Commerce Co., Ltd.
Effective date
2024-03-11
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
XIMONTH Bee Venom Pain CreamShantou Youjia E-Commerce Co., Ltd.2024-03-11HUMAN OTC DRUG LABEL

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 3 of 3 · 43 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
D2 Organ SupportSOLIDAGO VIRGAUREA, BAPTISIA TINCTORIA, BERBERIS VULGARIS, EQUISETUM HYEMALE, ARGENTUM NITRICUM, CANTHARIS, CAPSICUM ANNUUM, CUPRUM SULPHURICUM, ORTHOSIPHON STAMINEUS, SARSAPARILLA (SMILAX REGELII), BAROSMA (BETULINA), MERCURIUS CORROSIVUS, PAREIRA BRAVA, PYELON (SUIS), TEREBINTHINA, URETER (SUIS), URETHRA (SUIS), URINARY BLADDER (SUIS), ACETALDEHYDE, HEPAR SULPHURIS CALCAREUM, NATRUM PYRUVICUM, QUERCETIN, COLIBACILLINUM CUM NATRUM MURIATICUM, APIS VENENUM PURUM, DYSENTERY BACILLUSDr. Donna Restivo DC560c8847-c1a3-490f-9c4e-07665c9385382023-01-10WarningsExact identifier
unii: 76013O881M
ALLERGY DROPSAPIS MELLIFICA, APISINUM, ALLIUM CEPA, EUPHRASIA, SABADILLA, EUPHORBIUM, PULSATILLA, HEDERA HELIX, HISTAMINUM.Be Well Medical dba Richard Clement Nutrition y Be Well Homeopathics285996bb-e33d-4982-8282-05283f4e4c792021-12-29WarningsExact identifier
unii: 76013O881M
Apis Mell.APIS MELL.True Botanica, LLC61bc5f4a-f0c0-47d9-9747-d6f9dbf758242021-01-24WarningsExact identifier
unii: 76013O881M

Reported adverse events (FAERS/openFDA)#

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