NDC 82652-030 - Diphen
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
- 82652-030
- Package NDCs from labels
- 82652-030-01
- Manufacturer
- Remedy Pack LLC | Safetec of America, Inc | Allegiant Health | LNK International Inc. | Granules India Limited | Ohm Laboratories
- Effective date
- 2022-07-11
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Diphen | Remedy Pack LLC | Safetec of America, Inc | Allegiant Health | LNK International Inc. | Granules India Limited | Ohm Laboratories | 2022-07-11 | HUMAN OTC DRUG LABEL |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 82652-030-01 | Diphen | 2 in 1 PACKET | TABLET | 6 | 25 mg | 1 |
DailyMed Dashboard NDC Coverage#
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 82652-030 | DIPHEN (BENZOCAINE, BENZALKONIUM CHLORIDE, LIDOCAINE HYDROCHLORIDE, HYDROCORTISONE, BACITRACIN ZINC, NEOMYCIN SULFATE, POLYMYXIN B SULFATE, CALCIUM CARBONATE, IBUPROFEN, LORATADINE, ACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE, GUAIFENESIN, PHENYLEPHRINE HYDROCHLORIDE, DIPHENHYDRAMINE HYDROCHLORIDE, POTASSIUM CHLORIDE, MAGNESIUM OXIDE, MECLIZINE HYDROCHLORIDE, AND BISMUTH SUBSALICYLATE) KIT [REMEDY PACK LLC] | 1 | Unmatched | 20220717_5d185f23-8af6-4e36-b514-5662986520a5.zip |
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.
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.