NDC 62011-0071-01 - Loratadine and Pseudoephedrine Sulfate
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
- 62011-0071
- Requested NDC
- 62011-0071-01
- Package NDCs from labels
- 62011-0071-2, 62011-0071-1, 62011-0071-01
- Manufacturer
- Strategic Sourcing Services LLC | Sun Pharmaceutical Industries Inc. | Ohm Laboratories Inc.
- Effective date
- 2024-11-22
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Drug Facts | Strategic Sourcing Services LLC | Sun Pharmaceutical Industries Inc. | Ohm Laboratories Inc. | 2024-11-22 | HUMAN OTC DRUG LABEL |
| Drug Facts | Strategic Sourcing Services LLC | Sun Pharmaceutical Industries Inc. | Ohm Laboratories Inc. | 2024-11-21 | HUMAN OTC DRUG LABEL |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 62011-0071-1 | Loratadine and Pseudoephedrine Sulfate | 10 in 1 BLISTER PACK | TABLET, FILM COATED, EXTENDED RE | 10 | 5 | |
| 62011-0071-2 | Loratadine and Pseudoephedrine Sulfate | 15 in 1 BLISTER PACK | TABLET, FILM COATED, EXTENDED RE | 15 | 5 |
DailyMed Dashboard NDC Coverage#
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 62011-0071 | LORATADINE AND PSEUDOEPHEDRINE SULFATE TABLET, FILM COATED, EXTENDED RELEASE [STRATEGIC SOURCING SERVICES LLC] | 5 | Current NDC, Legacy NDC, 1 package rows | 20241123_48bfc938-d97d-4b49-8637-3b00ac870902.zip |
| 62011-0071 | LORATADINE AND PSEUDOEPHEDRINE SULFATE TABLET, FILM COATED, EXTENDED RELEASE [STRATEGIC SOURCING SERVICES LLC] | 5 | Current NDC, Legacy NDC, 1 package rows | 20241123_cdecad62-bf1e-43fb-b4be-8fc54b63e4ae.zip |
DailyMed Billing Units#
| Package NDC | Billing unit | Product NDC | DailyMed indexing SPL | SPL version | Effective |
|---|---|---|---|---|---|
| 62011-0071-1 | EA - Each | 62011-0071 | cf52c418-ca82-42f1-b496-6f064a51b458 | 1 | 2013-02-13 |
| 62011-0071-2 | EA - Each | 62011-0071 | 1e1c366c-ae3e-4271-a99e-69ba07bbf210 | 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 |
|---|---|---|---|---|---|---|
| Dual Action Complete | FAMOTIDINE, CALCIUM CARBONATE, MAGNESIUM HYDROXIDE | H E B | ea712fc4-7f27-4556-b1b8-028f3f6ce57a | 2025-07-07 | Warnings | H0G9379FGK |
| DG Health acid reducer complete | FAMOTIDINE, CALCIUM CARBONATE AND MAGNESIUM HYDROXIDE | Dolgencorp, LLC | 95c2c515-0f31-49d9-b799-7aaded81a37c | 2025-07-07 | Warnings | H0G9379FGK |
| Mineral Lip Sunscreen | TITANIUM DIOXIDE, ZINC OXIDE | CAPE COD SKIN CARE CO. INC. | 39093b2d-3fbb-8378-e063-6294a90ac6d8 | 2025-07-03 | 15FIX9V2JP | |
| Nuvicare-Allergy Relief Loratadine Tablets, 10 mg | LORATADINE | NUVICARE LLC | 023a46f0-8d1c-4f62-953d-3e6458a54f6e | 2025-07-01 | Warnings | 7AJO3BO7QN |
| topcare dual action complete | FAMOTIDINE, CALCIUM CARBONATE AND MAGNESIUM HYDROXIDE | Topco Associates LLC | 8ef70327-9a04-413b-b331-f5d3a94d6b36 | 2025-07-01 | Warnings | H0G9379FGK |
| KOSHER MEDS antacid | CALCIUM CARBONATE | Mollec Inc | 7783d6a2-56e3-4542-ad1d-60680e03532b | 2025-07-01 | Warnings | H0G9379FGK |
| Acid Reducer Complete | FAMOTIDINE, CALCIUM CARBONATE AND MAGNESIUM HYDROXIDE | Walgreen Company | 3a456dab-0a2d-4e48-a8e2-e49a7acef963 | 2025-07-01 | Warnings | H0G9379FGK |
| Dual Action Complete | FAMOTIDINE, CALCIUM CARBONATE AND MAGNESIUM HYDROXIDE | H E B | c1aa7efa-4be1-4c8f-8994-661dd60e1aa9 | 2025-07-01 | Warnings | H0G9379FGK |
| leader acid reducer complete | FAMOTIDINE, CALCIUM CARBONATE AND MAGNESIUM HYDROXIDE | Cardinal Health 110, LLC. dba Leader | a5420ef1-313f-4561-baf1-7ae017ea343a | 2025-07-01 | Warnings | H0G9379FGK |
| Arnica Calendula Wound | ARNICA CALENDULA WOUND | Uriel Pharmacy, Inc | 38cfd292-4dbd-2caf-e063-6394a90a0527 | 2025-06-30 | Warnings | ETJ7Z6XBU4 |
| Bac | APIS MELLIFERA, ARSENIC TRIOXIDE, ATROPA BELLADONNA, MATRICARIA CHAMOMILLA FLOWERING TOP OIL, LACHESIS MUTA VENOM, MERCURIUS SOLUBILIS, PULSATILLA VULGARIS WHOLE, TOXICODENDRON PUBESCENS LEAF, AND SILICON DIOXIDE | Zorex | 7ae38e0c-8e74-4fd5-8605-45e424a84d01 | 2025-06-30 | Warnings | ETJ7Z6XBU4 |
| Gencare-Allergy Relief Loratadine Tablets, 10 mg | LORATADINE | Pioneer Life Sciences, LLC | 647dc957-4aee-48f6-bb77-e82d3b380e80 | 2025-06-30 | Warnings | 7AJO3BO7QN |
| Vertra S Dorian Kona Gold Signature Face Stick SPF 38 | TITANIUM DIOXIDE | Toshiki Pigment Co., ltd. | b7162a2f-07f1-6188-e053-2995a90a8a9c | 2025-06-27 | Warnings | 15FIX9V2JP |
| Bambusa Aurum | BAMBUSA AURUM | Uriel Pharmacy Inc. | 43f3dd30-701f-4fa4-9743-d10051c6e6d4 | 2025-06-27 | Warnings | ETJ7Z6XBU4 |
| Steritalc 2g | TALC | Novatech SA | c94e51d9-beef-4b06-e053-2a95a90a754a | 2025-06-25 | Warnings, Adverse reactions | 7SEV7J4R1U |
| MELAO WHITENING SUNSCREEN | TITANIUM DIOXIDE | Guangdong Aimu Biological Technology Co., Ltd | 1aaf5942-ff13-ee07-e063-6394a90acd28 | 2025-06-25 | Warnings | 15FIX9V2JP |
| BISUTANG Sunscreen | BISUTANG SUNSCREEN | Guangdong Bisutang Biotechnology Co Ltd | 37fdb01b-929e-6a60-e063-6394a90a94e0 | 2025-06-20 | 15FIX9V2JP | |
| Double Use Compact SPF 15 gold deluxe edition Claire 1-2-3 | OCTINOXATE, TITANIUM DIOXIDE, ZINC OXIDE | Bel Star S.A. (Colombia) | b3747373-ef67-89ff-e053-2995a90afcde | 2025-06-20 | Warnings | 15FIX9V2JP |
| LBEL DIVINE Double Use compact SPF 15 gold deluxe edition Obscure 8-9 | ZINC OXIDE, TITANTIUM DIOXIDE, OCTINOXATE | Bel Star S.A. (Colombia) | b5e47c63-7e82-34fc-e053-2a95a90a767c | 2025-06-20 | Warnings | 15FIX9V2JP |
| Pepcid Complete | FAMOTIDINE, CALCIUM CARBONATE, AND MAGNESIUM HYDROXIDE | Morning Star OTC | be7f97d5-d2f2-45a8-96b4-fed1549ae2a3 | 2025-06-19 | Warnings | H0G9379FGK |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.