NDC 66715-9733-03 - Advil PM
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
- 66715-9733
- Requested NDC
- 66715-9733-03
- Package NDCs from labels
- 66715-9733-2, 66715-9733-8, 66715-9733-3, 66715-9733-03
- Manufacturer
- Lil' Drug Store Products, Inc.
- Effective date
- 2024-11-27
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Advil ® PM Lil' Drug Store ® , TRAVEL BASIX, CVP ® HEALTH | Lil' Drug Store Products, Inc. | 2024-11-27 | HUMAN OTC DRUG LABEL |
FDA-Initiated Inactive NDC Indexing#
| NDC | Effective | Action | Document | Indexing SPL | Related label |
|---|---|---|---|---|---|
| 66715-9733-2 | 2024-01-30 | C162847 | 48780-1 | 1030e365-636a-111a-e063-dadaa90a10e2 | Advil ® PM Lil' Drug Store ® , TRAVEL BASIX, CVP ® HEALTH |
| 66715-9733-3 | 2024-01-30 | C162847 | 48780-1 | 1030e365-636a-111a-e063-dadaa90a10e2 | Advil ® PM Lil' Drug Store ® , TRAVEL BASIX, CVP ® HEALTH |
| 66715-9733-8 | 2024-01-30 | C162847 | 48780-1 | 1030e365-636a-111a-e063-dadaa90a10e2 | Advil ® PM Lil' Drug Store ® , TRAVEL BASIX, CVP ® HEALTH |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 66715-9733-2 | Advil PM | 2 in 1 CARTON | TABLET, COATED | 2 | 12 | |
| 66715-9733-2 | Advil PM | 2 in 1 POUCH | TABLET, COATED | 2 | 12 | |
| 66715-9733-3 | Advil PM | 3 in 1 CARTON | TABLET, COATED | 3 | 12 | |
| 66715-9733-3 | Advil PM | 2 in 1 POUCH | TABLET, COATED | 2 | 12 | |
| 66715-9733-8 | Advil PM | 2 in 1 POUCH | TABLET, COATED | 2 | 12 | |
| 66715-9733-8 | Advil PM | 5 in 1 CARTON | TABLET, COATED | 5 | 12 |
DailyMed Dashboard NDC Coverage#
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 66715-9733 | ADVIL PM (IBUPROFEN AND DIPHENHYDRAMINE CITRATE) TABLET, COATED ADVIL PM, TRAVEL BASIX (IBUPROFEN AND DIPHENHYDRAMINE CITRATE) TABLET, COATED ADVIL PM, CVP HEALTH (IBUPROFEN AND DIPHENHYDRAMINE CITRATE) TABLET, COATED [LIL' DRUG STORE PRODUCTS, INC.] | 12 | Current NDC, Legacy NDC, 6 package rows | 20241219_b876bb40-a38b-445a-bc8a-466b3bfe166d.zip |
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 |
|---|---|---|---|---|---|---|
| Lymph Tonic II | ECHINACEA (ANGUSTIFOLIA), COLLINSONIA CANADENSIS, PHYTOLACCA DECANDRA, KALI IODATUM, PINUS SYLVESTRIS, PIX LIQUIDA, FERRUM PHOSPHORICUM, AESCULUS HIPPOCASTANUM, BARYTA CARBONICA, BERBERIS VULGARIS, CALCAREA CARBONICA, CALCAREA PHOSPHORICA, CAUSTICUM, HEPAR SULPHURIS CALCAREUM, KREOSOTUM, LYCOPODIUM CLAVATUM, MERCURIUS SOLUBILIS, NATRUM MURIATICUM, NITRICUM ACIDUM, PHOSPHORUS, PULSATILLA (PRATENSIS), SILICEA, STELLARIA MEDIA, SULPHUR, TEREBINTHINA, THUJA OCCIDENTALIS, BUFO RANA | BioActive Nutritional, Inc. | 0e3265b0-b210-4a4c-80d2-8a9712981d4e | 2026-09-17 | Warnings | ETJ7Z6XBU4 |
| dual action | ACETAMINOPHEN, IBUPROFEN | Rite Aid Corporation | 54b08d24-d5e9-4111-9d97-329896e8309d | 2026-09-09 | Warnings | WK2XYI10QM |
| Stay Ageless Tinted Mineral Sunscreen | BROAD SPECTRUM SPF30 | W Aesthetics | 5b0f2c8f-d6fa-5e25-e063-6394a90a084d | 2026-09-09 | Warnings | 15FIX9V2JP |
| Ibuprofen | IBUPROFEN | Lidl US LLC | 0ca02f8b-4413-4e7c-a67b-8c67c53e1343 | 2026-09-09 | Warnings | WK2XYI10QM |
| Ibuprofen | IBUPROFEN | GOODSENSE | 596a1007-08ea-00ec-e063-6394a90a5eb2 | 2026-09-09 | Warnings | WK2XYI10QM |
| ibuprofen childrens | IBUPROFEN | Rite Aid Corporation | c6e68886-edcb-414d-9cba-0d97772ef8b6 | 2026-09-09 | Warnings | WK2XYI10QM |
| Ibuprofen minis | IBUPROFEN | The Kroger Co. | 15709fa7-114b-453c-b63d-f1c4f28f0f95 | 2026-09-08 | Warnings | WK2XYI10QM |
| Ibuprofen | IBUPROFEN | REMEDYREPACK INC. | 2144eff0-d7ab-486d-b116-a4ff3ae2afe2 | 2026-09-08 | Boxed warning, Warnings, Adverse reactions | WK2XYI10QM |
| Ibuprofen | IBUPROFEN | The Kroger Co. | a7789f7f-3356-463b-9fd7-2d7f7eba2799 | 2026-09-08 | Warnings | WK2XYI10QM |
| IBUPROFEN | IBUPROFEN | Amazon.com Services LLC | 90659e83-d989-46a5-9680-3a4f61612511 | 2026-09-04 | Warnings | WK2XYI10QM |
| Ibuprofen | IBUPROFEN | Direct_Rx | 40071818-5bf0-095b-e063-6294a90ad58a | 2026-09-04 | Boxed warning, Warnings, Adverse reactions | WK2XYI10QM |
| Psoriasis Control | CENTELLA ASIATICA, SODIUM CHLORIDE, AND SILICON DIOXIDE | Forces of Nature | 2db33771-0bb9-49f8-84fa-dddc28e4ba26 | 2026-09-04 | Warnings | ETJ7Z6XBU4 |
| Ibuprofen | IBUPROFEN | Chain Drug Marketing Association, Inc. | 8d518a08-486a-4d11-b042-27fc1e6060c9 | 2026-09-03 | Warnings | WK2XYI10QM |
| IBUPROFEN Immediate Release | IBUPROFEN | Strides Pharma Inc | a5dd275f-f388-44ec-8297-74430a742d52 | 2026-09-02 | Boxed warning, Warnings | WK2XYI10QM |
| Ibuprofen | IBUPROFEN | PD-Rx Pharmaceuticals, Inc. | 0fa4cd66-66ad-4ec9-b38c-6b5840df39df | 2026-09-02 | Boxed warning, Warnings, Adverse reactions | WK2XYI10QM |
| Ibuprofen Immediate Release | IBUPROFEN | Strides Pharma Inc | ebcc4da3-d0f6-4e40-99b5-e88310ea4a5b | 2026-09-02 | Boxed warning, Warnings | WK2XYI10QM |
| Ibuprofen | IBUPROFEN | REMEDYREPACK INC. | 99730c4a-d2ee-46f5-91f4-a15cbaace40d | 2026-09-01 | Boxed warning, Warnings, Adverse reactions | WK2XYI10QM |
| Ibuprofen | IBUPROFEN | PD-Rx Pharmaceuticals, Inc. | 3a38add6-a114-4e18-836c-3bfc727db231 | 2026-09-01 | Boxed warning, Warnings, Adverse reactions | WK2XYI10QM |
| Ibuprofen | IBUPROFEN | REMEDYREPACK INC. | 404df13d-4ada-4324-9eed-e21f5d5043a4 | 2026-09-01 | Boxed warning, Warnings, Adverse reactions | WK2XYI10QM |
| Ibuprofen | IBUPROFEN | Shield Pharmaceuticals Corp | fef89d3f-16e1-4a76-aabd-11d6eca4be86 | 2026-09-01 | Warnings | WK2XYI10QM |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.