NDC 69842-324 - CVS
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
- 69842-324
- Package NDCs from labels
- 69842-324-01
- Manufacturer
- CVS Pharmacy, Inc.
- Effective date
- 2025-02-03
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| CVS Soft Tip Squeeze Sinus Wash System | CVS Pharmacy, Inc. | 2025-02-03 | HUMAN OTC DRUG LABEL |
| CVS - CVS Pharmacy | CVS Pharmacy | 2025-02-03 | HUMAN OTC DRUG LABEL |
| CVS- Allergy relief Netipot | CVS Pharmacy, Inc. | 2025-02-03 | HUMAN OTC DRUG LABEL |
| CVS - CVS Pharmacy | CVS Pharmacy | 2025-01-31 | HUMAN OTC DRUG LABEL |
| CVS Instant Relief Ready to Use Sinus Wash System | CVS Pharmacy, Inc. | 2020-06-08 | HUMAN OTC DRUG LABEL |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 69842-324-01 | CVS | 3000 mg in 1 PACKET | POWDER | 3000 mg | 22.8 mg in 100mg | 7 |
| 69842-324-01 | CVS | 3000 mg in 1 PACKET | POWDER | 3000 mg | 77.8 mg in 100mg | 6 |
| 69842-324-01 | CVS | 3000 mg in 1 PACKET | POWDER | 3000 mg | 77.8 mg in 100mg | 4 |
| 69842-324-01 | CVS | 3000 mg in 1 PACKET | POWDER | 3000 mg | 77.8 mg in 100mg | 2 |
DailyMed Dashboard NDC Coverage#
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 69842-324 | CVS (SODIUM CHLORIDE, SODIUM BICARBONATE) KIT [CVS PHARMACY, INC.] | 7 | Unmatched | 20250205_fe2ac0d1-18d4-4cff-833d-5e5eab783352.zip |
| 69842-324 | CVS (SODIUM CHLORIDE, SODIUM BICARBONATE) KIT [CVS PHARMACY] | 6 | Unmatched | 20250205_a7831b84-1f4d-9258-e053-2a95a90a901e.zip |
| 69842-324 | CVS (SODIUM CHLORIDE, SODIUM BICARBONATE) KIT [CVS PHARMACY] | 4 | Unmatched | 20250205_a0ac34cd-b256-4f69-b506-22ebf5726f68.zip |
| 69842-324 | CVS (SODIUM CHLORIDE, SODIUM BICARBONATE) KIT [CVS PHARMACY, INC.] | 2 | Unmatched | 20250205_a782735a-862b-7173-e053-2995a90ad85d.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.
| Brand | Generic | Manufacturer | SPL set ID | Effective date | Available safety fields | Join |
|---|---|---|---|---|---|---|
| Crane Safety Eye Wash | WATER SOLUTION | Crane Safety LLC | 96d8dda9-6cd6-3f68-e053-2995a90a0da2 | 2024-11-08 | Warnings | 059QF0KO0R |
| RUGBY EYE WASH | WATER, PURIFIED | A-S Medication Solutions | 0773e558-2f46-494c-888a-3bc517202b65 | 2024-11-08 | Warnings | 059QF0KO0R |
| Dove | MEN SKIN DEFENSE ANTIBACTERIAL 3N1 HAND BODY SHAVE BAR | Conopco Inc. d/b/a/ Unilever | b9e61a03-e000-50ab-e053-2a95a90a3210 | 2024-11-07 | Warnings | F5UM2KM3W7 |
| Dove | DOVE CARE AND PROTECT ANTIBACTERIAL NOURISHING FOAMING HAND WASH | Conopco Inc. d/b/a/ Unilever | b9f8cb31-560c-79e0-e053-2a95a90a39ae | 2024-11-07 | Warnings | F5UM2KM3W7 |
| Dove | CARE AND PROTECT ANTIBACTERIAL HAND WASH | Conopco Inc. d/b/a/ Unilever | ed234413-777a-9c82-e053-2a95a90a6f98 | 2024-11-07 | Warnings | F5UM2KM3W7 |
| Dove | CARE AND PROTECT ANTIBACTERIAL FOAMING HAND WASH | Conopco Inc. d/b/a/ Unilever | ed24b320-27fc-9714-e053-2995a90a79a6 | 2024-11-07 | Warnings | F5UM2KM3W7 |
| Nice n Clean Wipes Sani-Hands Antibacterial Hand Wipes | BENZALKONIUM CHLORIDE HAND WIPES | Nice-Pak Products, Inc. | b6e6577c-c172-f3df-e053-2a95a90ac515 | 2024-11-07 | Warnings | F5UM2KM3W7 |
| Sodium Bicarbonate | SODIUM BICARBONATE | Cardinal Health 107, LLC | f7c88834-aa7c-4aaa-ab9b-0cbcd1f4da3f | 2024-11-07 | Warnings | 8MDF5V39QO |
| Dextrose and Sodium Chloride | DEXTROSE MONOHYDRATE AND SODIUM CHLORIDE | BECTON DICKINSON AND COMPANY | d3f90d2f-4536-4d32-800b-7a798f8a35db | 2024-11-07 | Warnings, Adverse reactions | 451W47IQ8X |
| Band Aid Antiseptic Cleansing To Go | BENZALKONIUM CHLORIDE, PRAMOXINE HCL | Kenvue Brands LLC | d5749cba-32f3-cf9c-e053-2a95a90a4416 | 2024-11-06 | Warnings | F5UM2KM3W7 |
| Sodium Chloride | SODIUM CHLORIDE | Hospira, Inc. | 8eb172da-dcd4-4660-4a8f-ad44a14b4af7 | 2024-11-06 | Adverse reactions | 451W47IQ8X |
| Alocane Max | LIDOCAINE HYDROCHLORIDE AND BENZALKONIUM CHLORIDE | Quest Products LLC | 0a35ac19-6883-a733-e063-6294a90ad22d | 2024-11-05 | Warnings | F5UM2KM3W7 |
| Alocane Plus | LIDOCAINE HYDROCHLORIDE AND BENZALKONIUM CHLORIDE | Quest Products, Inc. | cfe8114b-df65-064b-e053-2a95a90a33f6 | 2024-11-05 | Warnings | F5UM2KM3W7 |
| Licefreee Everyday | SODIUM CHLORIDE | Tec Laboratories,Inc. | 407b5fd6-2331-2ba7-e054-00144ff88e88 | 2024-11-05 | Warnings | 451W47IQ8X |
| Antibacterial Lidocaine Wound Gel | BENZALKONIUM CHLORIDE, LIDOCAINE HYDROCHLORIDE | ASO LLC | cb9505b7-222d-3a24-e053-2a95a90a0b64 | 2024-11-05 | Warnings | F5UM2KM3W7 |
| Licefreee | HEAD LICE TREATMENT | Tec Laboratories, Inc. | 08c9d3dd-7177-0148-e054-00144ff8d46c | 2024-11-05 | Warnings | 451W47IQ8X |
| Bladder Relief | CAUSTICUM, NATRUM MURIATICUM, NUX VOMICA, PULSATILLA (VULGARIS), SEPIA, STAPHYSAGRIA, THUJA OCCIDENTALIS | Magni Company | 5d0db70c-6360-493b-bcf2-8dbc95314140 | 2024-11-05 | Warnings | 451W47IQ8X |
| Altra Antimicrobial Foaming Hand Wash w/ Benzalkonium Chloride | BENZALKONIUM CHLORIDE | Buckeye International, Inc. | 2618ecdc-3eeb-a69b-e063-6394a90a8024 | 2024-11-04 | Warnings | F5UM2KM3W7 |
| Vaccines | ARNICA MONTANA, HYPERICUM PERFORATUM, LEDUM PALUSTRE, MORBILLINUM, NATRUM MURIATICUM, SILICEA, SULPHUR IODATUM, THUJA OCCIDENTALIS, URTICA URENS | Liddell Laboratories, Inc. | 6e6e67d4-089e-4775-b4a4-5511953f6e3f | 2024-11-04 | Warnings | 451W47IQ8X |
| Gluten Detox | BARLEY (GRAIN), CARBO VEGETABILIS, CINCHONA OFFICINALIS, GLUTEN, GLYPHOSATE, HYDRASTIS CANADENSIS, LYCOPODIUM CLAVATUM, NATRUM MURIATICUM, NUX VOMICA, OAT (GRAIN), PANCREAS SUIS, PULSATILLA (VULGARIS), RYE (GRAIN), WHEAT (GRAIN) | Liddell Laboratories, Inc. | 706f2e33-8674-4911-ba0a-4efc935e7739 | 2024-11-04 | Warnings | 451W47IQ8X |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.