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 | Type |
|---|---|---|---|
| XIMONTH Bee Venom Pain Cream | Shantou Youjia E-Commerce Co., Ltd. | 2024-03-11 | HUMAN 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.
| Brand | Generic | Manufacturer | SPL set ID | Effective date | Available safety fields | Join |
|---|---|---|---|---|---|---|
| D2 Organ Support | SOLIDAGO 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 BACILLUS | Dr. Donna Restivo DC | 560c8847-c1a3-490f-9c4e-07665c938538 | 2023-01-10 | Warnings | 76013O881M |
| ALLERGY DROPS | APIS MELLIFICA, APISINUM, ALLIUM CEPA, EUPHRASIA, SABADILLA, EUPHORBIUM, PULSATILLA, HEDERA HELIX, HISTAMINUM. | Be Well Medical dba Richard Clement Nutrition y Be Well Homeopathics | 285996bb-e33d-4982-8282-05283f4e4c79 | 2021-12-29 | Warnings | 76013O881M |
| Apis Mell. | APIS MELL. | True Botanica, LLC | 61bc5f4a-f0c0-47d9-9747-d6f9dbf75824 | 2021-01-24 | Warnings | 76013O881M |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.