NDC 47682-808-99 - Mountain Series Weekender Medical
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
- 47682-808
- Requested NDC
- 47682-808-99
- Package NDCs from labels
- 47682-808-99
- Manufacturer
- Tender Corporation dba Adventure Medical Kits
- Effective date
- 2011-08-01
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Antiseptic Towelette - Tender Corporation dba Adventure Medical Kits | Tender Corporation dba Adventure Medical Kits | 2011-08-01 | HUMAN OTC DRUG LABEL |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 47682-808-99 | Mountain Series Weekender Medical | 2 in 1 PACKET | TABLET, FILM COATED | 2 | 200 mg | 1 |
DailyMed Dashboard NDC Coverage#
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 47682-808 | MOUNTAIN SERIES WEEKENDER MEDICAL (BENZALKONIUM CHLORIDE, POVIDONE-IODINE, ACETAMINOPHEN, ASPIRIN, DIPHENHYDRAMINE HYDROCHLORIDE, IBUPROFEN, BACITRACIN ZINC, NEOMYCIN SULFATE, POLYMYXIN B SULFATE) KIT [TENDER CORPORATION DBA ADVENTURE MEDICAL KITS] | 1 | Unmatched | 20110801_e4b05cbc-526e-4a03-a943-631a0feb6947.zip |
DailyMed Billing Units#
| Package NDC | Billing unit | Product NDC | DailyMed indexing SPL | SPL version | Effective |
|---|---|---|---|---|---|
| 47682-808-13 | EA - Each | 47682-808 | 0f9bb74d-9e95-402b-b680-33dfc130fe88 | 1 | 2012-07-24 |
| 47682-808-30 | EA - Each | 47682-808 | 7a51b6b0-cc50-4923-b5db-b246a975188a | 1 | 2015-10-02 |
| 47682-808-33 | EA - Each | 47682-808 | 40cc5d6b-7fc4-42f7-838c-1a401b8942e0 | 1 | 2012-07-24 |
| 47682-808-48 | EA - Each | 47682-808 | 5b1e19d4-e0e7-4437-a841-c419c32daa60 | 1 | 2013-03-03 |
| 47682-808-99 | EA - Each | 47682-808 | 3d91a842-9124-42ce-94b8-26aa91dd9d84 | 1 | 2018-03-08 |
DailyMed Socrata Ingredients#
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 |
|---|---|---|---|---|---|---|
| KUGIG ALOE FOAMING INTIMATE WASH | INTIMATE CLEANSING FOAM | Hong Kong KangXing Centennial Management Limited | 59f4d398-1186-a168-e063-6294a90ab44b | 2026-08-26 | Warnings | 059QF0KO0R |
| Argentum Quartz | ARGENTUM QUARTZ | Uriel Pharmacy Inc. | 765c8c8f-0727-45da-a77e-c3907a3d0793 | 2026-08-26 | Warnings | ETJ7Z6XBU4 |
| Endometrium Argentum | ENDOMETRIUM ARGENTUM | Uriel Pharmacy Inc | d2d1428a-c8b5-9529-e053-2995a90a2343 | 2026-08-26 | Warnings | ETJ7Z6XBU4 |
| S12 AIRBORNE | ALFALFA, ALLIUM SATIVUM, ARSENICUM IODATUM, BARLEY, BETULA PUBESCENS, BROWN RICE, CORN GRAIN, EUPHRASIA OFFICINALIS, FEATHER MIX, HAIR MIX, HISTAMINUM, HOUSE DUST MITE, LOLIUM PERENNE, OAT, PERFOLIATE HONEYSUCKLE, PHLEUM PRATENSE, POLLEN MIX, RYE, SABADILLA, SILICEA, SKIN MIX, SOLIDAGO VIRGAUREA, TARAXACUM OFFICINALE, TEREBINTHINA, WHEAT | Apex Energetics Inc. | bb0036c3-1e4d-5750-e053-2995a90ae895 | 2026-08-26 | Warnings | ETJ7Z6XBU4 |
| Daytime Cold and Flu mini Softgels | ACETAMINOPHEN, DEXTROMETHORPHAN HBR, PHENYLEPHRINE HCL | Shield Pharmaceuticals Corp | dfb0fe2e-b0c7-409a-bd1a-fd12485665ba | 2026-08-26 | Warnings | 362O9ITL9D |
| Povidone Iodine Swabstick | POVIDONE IODINE 10% | Trifecta Pharmaceuticals USA LLC | 59f82f9d-8c39-6890-e063-6294a90a090e | 2026-08-26 | Warnings | 85H0HZU99M |
| Mercurochrome | BENZALKONIUM CHLORIDE | Vitamex USA, Corp | 21652b11-715d-0c54-e063-6294a90a8855 | 2026-08-26 | Warnings | F5UM2KM3W7 |
| Biopure Antibacterial Hand Wipe | ANTIBACTERIAL HAND WIPE | Fujian Yifa Healthcare Products Co., Ltd. | 59fa27b4-dfd4-720b-e063-6394a90af659 | 2026-08-26 | Warnings | F5UM2KM3W7 |
| Biopure Antibacterial Hand Wipe | ANTIBACTERIAL HAND WIPE | Fujian Yifa Healthcare Products Co., Ltd. | 59fb22d6-f6a4-42cd-e063-6394a90a859a | 2026-08-26 | Warnings | F5UM2KM3W7 |
| Biopure Antibacterial Hand Wipe | ANTIBACTERIAL HAND WIPE | Fujian Yifa Healthcare Products Co., Ltd. | 59fbb054-461e-aa6e-e063-6394a90a470c | 2026-08-26 | Warnings | F5UM2KM3W7 |
| Nighttime Severe Cold and Flu Maximum Strength mini softgels | ACETAMINOPHEN, DEXTROMETHORPHAN HBR, DOXYLAMINE SUCCINATE, PHENYLEPHRINE HCL | Shield Pharmaceuticals Corp | 70c5517d-be4e-4317-b4f4-df660c71c699 | 2026-08-26 | Warnings | 362O9ITL9D |
| Childrens Pain and Fever | ACETAMINOPHEN | FSA STORE INC. | 5502ef15-9f40-db56-e063-6394a90a2de4 | 2026-08-26 | Warnings | M013 362O9ITL9D |
| foster and thrive dual action | ACETAMINOPHEN, IBUPROFEN | Strategic Sourcing Services LLC | f970d423-1d92-40c0-8358-91d1f963505c | 2026-08-26 | Warnings | WK2XYI10QM 362O9ITL9D |
| DG Health 8 Hour Pain Relief | ACETAMINOPHEN | Dolgencorp Inc | d102e8a2-2fff-48cb-9864-7582fde956ed | 2026-08-26 | Warnings | 362O9ITL9D |
| Cold and Flu | ACETAMINOPHEN, DEXTROMETHORPHAN HBR, GUAIFENESIN, PHENYLEPHRINE HCL | Meijer Distribution, Inc. | c1f9ec75-7eb2-405c-8cdc-097cbf2cf87d | 2026-08-26 | Warnings | 362O9ITL9D |
| Pain Reliever | ACETAMINOPHEN, IBUPROFEN | CVS Pharmacy | 9126e680-d5ff-4189-9f9a-d797822ce670 | 2026-08-26 | Warnings | WK2XYI10QM 362O9ITL9D |
| Leader Dual Action Pain Reliever | ACETAMINOPHEN, IBUPROFEN | Cardinal Health 110, LLC. dba Leader | 2bb1f616-48af-4fe1-9aa9-32fcb2dba50c | 2026-08-26 | Warnings | WK2XYI10QM 362O9ITL9D |
| Dye Free Pain and Fever Childrens | ACETAMINOPHEN | Walgreens | 3ea217dd-e5b9-4d4b-861a-76ce61ba3a1d | 2026-08-26 | Warnings | M013 362O9ITL9D |
| dual pain reliever | ACETAMINOPHEN, IBUPROFEN | Walgreen Company | 5cb3b0b4-5b47-4ed4-a5e3-f14dbbcb46df | 2026-08-26 | Warnings | WK2XYI10QM 362O9ITL9D |
| Infants Ibuprofen | IBUPROFEN | Walgreens | 3bbbe142-a00c-404b-a116-81ad730ea130 | 2026-08-25 | Warnings | WK2XYI10QM |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.