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 |
|---|---|---|---|---|---|---|
| severe cold and flu relief | ACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE, DOXYLAMINE SUCCINATE, PHENYLEPHRINE HYDROCHLORIDE | Rite Aid Corporation | 4b8ae971-ab57-4937-a878-72d905d7b849 | 2026-09-09 | Warnings | 362O9ITL9D |
| Cold and Flu Relief | ACETAMINOHPEN, DEXTROMETHORPHAN HBR, PHENYLEPHRINE HCL | CARDINAL HEALTH 110, LLC. DBA LEADER 70000 | 82ba9a73-60ef-49fd-960f-5ca2bb79555e | 2026-09-09 | Warnings | 362O9ITL9D |
| DRx Choice maximum strength Severe Cough plus sore throat | ACETAMINOPHEN, DEXTROMETHORPHAN HBR | RARITAN PHARMACEUTICALS | a096cb76-0d1c-4ca8-854a-5199da0bc8f7 | 2026-09-09 | Warnings | 362O9ITL9D |
| Acetaminophen Extra Strength | ACETAMINOPHEN | Wal-Mart Stores Inc | 78874258-16cc-40b5-9e15-5943eddfce94 | 2026-09-08 | Warnings | M013 362O9ITL9D |
| Ibuprofen | IBUPROFEN | REMEDYREPACK INC. | 2144eff0-d7ab-486d-b116-a4ff3ae2afe2 | 2026-09-08 | Boxed warning, Warnings, Adverse reactions | WK2XYI10QM |
| Vicks DayQuil VapoCOOL SEVERE COLD and FLU plus CONGESTION | ACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE, GUAIFENESIN, AND PHENYLEPHRINE HYDROCHLORIDE | The Procter & Gamble Manufacturing Company | efb69cc1-a745-6efc-e053-2a95a90abdc9 | 2026-09-08 | Warnings | 362O9ITL9D |
| Vicks NyQuil VapoCOOL Severe COLD and FLU plus CONGESTION | ACETAMINOPHEN, PHENYLEPHRINE HYDROCHLORIDE, DOXYLAMINE SUCCINATE, AND DEXTROMETHORPHAN HYDROBROMIDE | The Procter & Gamble Manufacturing Company | efb5f0b9-9825-ab23-e053-2995a90a26ab | 2026-09-08 | Warnings | 362O9ITL9D |
| VICKS ZzzQuil NIGHTTIME SLEEP-AID Diphenhydramine HCl FREE OF | DIPHENHYDRAMINE HYDROCHLORIDE | The Procter & Gamble Manufacturing Company | 01906eed-78ee-f2a1-e063-6294a90a809b | 2026-09-08 | Warnings | TC2D6JAD40 |
| Overnight Cold and Flu | ACETAMINOPHEN, DEXTROMETHORPHAN HBR, TRIPROLIDINE HCL | RARITAN PHARMACEUTICALS | eef00453-9f4f-4a05-bb4e-49b94705b52c | 2026-09-08 | Warnings | 362O9ITL9D |
| Pain and Fever Childrens | ACETAMINOPHEN | DOLGENCORP, LLC | c637b39c-a049-43af-a582-fc242e940d85 | 2026-09-08 | Warnings | M013 362O9ITL9D |
| Nighttime Severe Cold and Cough | ACETAMINOPHEN, DIPHENHYDRAMINE, PHENYLEPHRINE | RARITAN PHARMACEUTICALS INC | 9819155b-2713-42be-867e-16605e7643d0 | 2026-09-08 | Warnings | TC2D6JAD40 362O9ITL9D |
| Pain Reliever Extra Strength | ACETAMINOPHEN | Walgreen Company | f7667529-09c0-4603-8080-f236144fac36 | 2026-09-08 | Warnings | M013 362O9ITL9D |
| UP AND UP CHILDRENS ACETAMINOPHEN | ACETAMINOPHEN | Target Corporation | e2989ead-7fdc-4295-bf94-423195775670 | 2026-09-08 | Warnings | M013 362O9ITL9D |
| Cold and Flu HBP | ACETAMINOPHEN, CHLORPHENIRAMINE MALEATE | WALMART INC. | f9d1dfd1-527f-491d-9188-14886ac70ced | 2026-09-08 | Warnings | 362O9ITL9D |
| Ibuprofen | IBUPROFEN | The Kroger Co. | a7789f7f-3356-463b-9fd7-2d7f7eba2799 | 2026-09-08 | Warnings | WK2XYI10QM |
| Pain Relief Extra Strength | ACETAMINOPHEN | Rite Aid Corporation | d846065a-5c39-4f4b-894c-4280acaaf4fa | 2026-09-08 | Warnings | M013 362O9ITL9D |
| severe cold and cough daytime | ACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE, PHENYLEPHRINE HYDROCHLORIDE | RARITAN PHARMACEUTICALS INC | 3ce8508e-7d9d-4413-858a-8f952e760c01 | 2026-09-08 | Warnings | 362O9ITL9D |
| Multi Symptom Severe Cold | ACETAMINOPHEN, DEXTROMETHORPHAN HBR, PHENYLEPHRINE HCL | RARITAN PHARMACEUTICALS INC | d9606c9a-31b1-4121-9870-809a05f5b68a | 2026-09-08 | Warnings | 362O9ITL9D |
| BZK Antiseptic Towelette | BENZALKONIUM CHLORIDE CLOTH | JINHUA JINGDI MEDICAL SUPPLIES CO., LTD | 57cd664e-f232-bd50-e063-6394a90ac139 | 2026-09-07 | Warnings | F5UM2KM3W7 |
| American Safety and First Aid Triple Antibiotic | BACITRACIN ZINC, NEOMYCIN SULFATE, POLYMYXIN B SULFATE | Orazen Inc | eb0df2da-1688-c477-e053-2995a90a74a2 | 2026-09-07 | Warnings | 204602 89Y4M234ES 057Y626693 19371312D4 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.