NDC 51662-1663-02 - AUVI-Q
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
- 51662-1663
- Requested NDC
- 51662-1663-02
- Package NDCs from labels
- 51662-1663-1, 51662-1663-2, 51662-1663-02
- Manufacturer
- HF Acquisition Co LLC, DBA HealthFirst
- Effective date
- 2024-10-08
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| AUVI-Q - HF Acquisition Co LLC, DBA HealthFirst | HF Acquisition Co LLC, DBA HealthFirst | 2024-10-08 | HUMAN PRESCRIPTION DRUG LABEL |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 51662-1663-1 | AUVI-Q | 0.3 mL in 1 DOSE PACK | INJECTION, SOLUTION | 0.3 | 1 | |
| 51662-1663-2 | AUVI-Q | 2 in 1 CARTON | INJECTION, SOLUTION | 2 | 1 |
DailyMed Dashboard NDC Coverage#
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 51662-1663 | AUVI-Q INJECTION, SOLUTION [HF ACQUISITION CO LLC, DBA HEALTHFIRST] | 1 | Current NDC, 2 package rows | 20241010_23fdb616-0c60-44fe-e063-6394a90ad8f1.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 |
|---|---|---|---|---|---|---|
| Epinephrine | EPINEPHRINE | BPI Labs, LLC | 5b5282a9-b149-4f0a-978e-5adbf48ec8aa | 2025-12-26 | Warnings, Adverse reactions | YKH834O4BH |
| Triple Allergy Defense | ALLIUM CEPA, AMBROSIA ARTEMISIIFOLIA, EUPHRASIA OFFICINALIS, GALPHIMIA GLAUCA, HISTAMINUM HYDROCHLORICUM, HYDRASTIS CANADENSIS, LEMNA MINOR, LUFFA OPERCULATA, NATRUM MURIATICUM, POLYPORUS PINICOLA, SABADILLA | Nenningers Naturals, LLC | e1459ef4-6980-4b2b-94c1-6c896a9cb6bd | 2025-12-25 | Warnings | 451W47IQ8X |
| Dr. Nenninger Cold and Sinus Solution | ALLIUM CEPA, HEPAR SULPHURIS CALCAREUM, HYDRASTIS CANADENSIS, KALI BICHROMICUM, KALI IODATUM, NATRUM MURIATICUM, PULSATILLA | Nenningers Naturals, LLC | 1e26b25c-5d93-4f69-aa9e-a187abd6d035 | 2025-12-25 | Warnings | 451W47IQ8X |
| Normal Salt | SODIUM CHLORIDE | GRAXCELL PHARMACEUTICAL, LLC | f3f09817-8a38-4aa1-956b-69d9cf695074 | 2025-12-25 | Warnings | 451W47IQ8X |
| ActivMend | ARNICA MONTANA, HYPERICUM PERFORATUM, LEDUM PALUSTRE, RHUS TOXICODENDRON, RUTA GRAVEOLENS, NATRUM MURATICUM | Cearna, Inc. | baefc5d4-a7e4-4ba2-e053-2995a90a4b86 | 2025-12-23 | Warnings | 451W47IQ8X |
| Kids Cold and Cough Daytime | CALCIUM SULFIDE,GOLDENSEAL,ONION,PHOSPHORUS,PULSATILLA VULGARIS, SODIUM CHLORIDE | Hyland's Consumer Health Inc. | e6118c79-b6d5-5c09-e053-2a95a90a30cf | 2025-12-19 | Warnings | 451W47IQ8X |
| 4 KIDS COLD N COUGH GRAPE FLAVOR | ONION, CALCIUM SULFIDE, GOLDENSEAL, SODIUM CHLORIDE, PHOSPHORUS, ANEMONE PULSATILLA, AND SULFUR | Hyland's Inc. | 798e2a4d-da2d-4bbd-a9b8-574490ef7357 | 2025-12-19 | Warnings | 451W47IQ8X |
| 4 Kids Cold and Cough Daytime | ONION, CALCIUM SULFIDE, SODIUM CHLORIDE, PHOSPHORUS, PULSATILLA VULGARIS, SULFUR, AND GOLDENSEAL | Hyland's Inc. | 804e0e7a-20eb-128b-e053-2991aa0aa82c | 2025-12-19 | Warnings | 451W47IQ8X |
| 4 Kids Cold and Cough Nighttime Natural Grape Flavor | ONION,ANEMONE PULSATILLA, PHOSPHORUS, GOLDENSEAL, CALCIUM SULFIDE, SODIUM CHLORIDE, SULFUR, MATRICARIA CHAMOMILLA AND ARABICA COFFEE BEAN | Hyland's Inc. | 7923e59a-f62c-44df-e053-2991aa0afc1e | 2025-12-19 | Warnings | 451W47IQ8X |
| Hair and Nail Tonic | AVENA, DNA, ELAEIS, GLANDULA SUPRARENALIS SUIS, HAMAMELIS, HEPAR SUIS, KALI SULPH, NAT MUR, NICOTINAMIDUM, PHOSPHORICUM AC, PITUITARUM POSTERIUM, RIBOFLAVINUM, THIAMINUM HYDROCHLORICUM, THUJA OCC, THYROIDINUM, URTICA UR. | Eight and Company L.L.C | 35bda785-b3a7-4928-aaea-27bf9fb6abb5 | 2025-12-18 | Warnings | 451W47IQ8X |
| epinephrine | EPINEPHRINE | GLENMARK PHARMACEUTICALS INC., USA | cc4ebb51-6020-4339-a36a-ec2380b7d28e | 2025-12-18 | Warnings, Adverse reactions | YKH834O4BH |
| Epinephrine | EPINEPHRINE | ProPharma Distribution | 384445ac-0696-e367-e063-6394a90a019f | 2025-12-18 | Warnings, Adverse reactions | YKH834O4BH |
| Sterile Water | WATER | ProPharma Distribution | 386a0a2f-4ff7-f128-e063-6294a90a7d4d | 2025-12-18 | Warnings, Adverse reactions | 059QF0KO0R |
| Adrenalin | EPINEPHRINE | ProPharma Distribution | 3eef2920-0129-6dc2-e063-6294a90ac22a | 2025-12-18 | Warnings, Adverse reactions | YKH834O4BH |
| Sodium Chloride | SODIUM CHLORIDE | ProPharma Distribution | 3f79fb8b-d0e8-db2a-e063-6394a90ac136 | 2025-12-18 | Warnings, Adverse reactions | 451W47IQ8X |
| Lidocaine Hydrochloride and Epinephrine | LIDOCAINE HYDROCHLORIDE AND EPINEPHRINE | ProPharma Distribution | 43048b6b-3c83-eef4-e063-6294a90a34cb | 2025-12-18 | Warnings, Adverse reactions | YKH834O4BH |
| Body Balance | ARALIA QUIN, ARNICA, AVENA, CARDUUS MAR, ELAEIS, GLANDULA SUPRARENALIS SUIS, NAT MUR, PHOSPHORICUM AC, THUJA OCC | Eight and Company L.L.C | 876cc0cf-c7a7-4656-adf9-1eff9bb62687 | 2025-12-18 | Warnings | 451W47IQ8X |
| epinephrine | EPINEPHRINE | GLENMARK PHARMACEUTICALS INC., USA | 01fd19cd-190c-4989-b733-60ba95941297 | 2025-12-18 | Warnings, Adverse reactions | YKH834O4BH |
| ADRENOPLEX | CHELIDONIUM MAJUS, ECHINACEA (ANGUSTIFOLIA), GLANDULA SUPRARENALIS BOVINE, SPLEEN (SUIS), CARDUUS MARIANUS, LYCOPODIUM CLAVATUM, NATRUM MURIATICUM, PHOSPHORICUM ACIDUM | BioActive Nutritional, Inc. | 3c53c23e-7654-4e46-acf1-edb0d605ff3b | 2025-12-18 | Warnings | 451W47IQ8X |
| Vermasode | ARTEMISIA VULGARIS, CHELIDONIUM MAJUS, GRANATUM, SPIGELIA ANTHELMIA, RATANHIA, ARSENICUM ALBUM, FERRUM METALLICUM, CALCAREA CARBONICA, CINA, GAERTNER BACILLUS, GRAPHITES, MERCURIUS DULCIS, NATRUM MURIATICUM, NATRUM PHOSPHORICUM, VERMIN NOSODE | Natural Creations, Inc | 180b5641-5692-42d4-8472-fdadccebd746 | 2025-12-18 | Warnings | 451W47IQ8X |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.