NDC 43406-0697-01 - FCS CP
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
- 43406-0697
- Requested NDC
- 43406-0697-01
- Package NDCs from labels
- 43406-0697-1, 43406-0697-01
- Manufacturer
- Natural Creations, Inc | OHM Pharma, inc
- Effective date
- 2025-12-10
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| FCS CP - Natural Creations, Inc | OHM Pharma, inc | Natural Creations, Inc | OHM Pharma, inc | 2025-12-10 | HUMAN OTC DRUG LABEL |
FDA-Initiated Inactive NDC Indexing#
| NDC | Effective | Action | Document | Indexing SPL | Related label |
|---|---|---|---|---|---|
| 43406-0697-1 | 2022-03-03 | C162847 | 48780-1 | d6a99b39-377c-a426-e053-dadaa90af4c2 | FCS CP |
| 43406-0697-1 | 2022-01-28 | C162847 | 48780-1 | d6a99b39-377c-a426-e053-dadaa90af4c2 | FCS CP |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 43406-0697-1 | FCS CP | 30 mL in 1 BOTTLE, DROPPER | LIQUID | 30 | 5 |
DailyMed Dashboard NDC Coverage#
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 43406-0697 | FCS CP (CORTICOTROPIN,GLUTAMICACID,MUCUNAPURIENSSEED,SEROTONIN,EPINEPHRINE,NIACINAMIDE,UBIDECARENONE,ADENOSINETRIPHOSPHATE,INSULINPORK,SUSSCROFAPARATHYROIDGLAND,SUSSCROFAPITUITARYGLAND,THIAMINEHYDROCHLORIDE,THYROID,UNSPECIFIED,ANHYDROUSCITRICACID,HERRINGSPERMDNA,SACCHAROMYCESCEREVISIAERNA,ANACARDIUMOCCIDENTALEFRUIT,ARSENICTRIOXIDE,ASPARTICACID,BARIUMCARBONATE,OYSTERSHELLCALCIUMCARBONATE,CRUDE,CLEMATISRECTAFLOWERINGTOP,LYCOPODIUMCLAVATUMSPORE,ANEMONEPULSATILLA,DATURASTRAMONIUM,SULFUR) LIQUID [NATURAL CREATIONS, INC] | 4 | Current NDC, Legacy NDC, 1 package rows | 20220304_cb69e9d6-62a6-4af0-8d2d-1e68b0830a20.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 |
|---|---|---|---|---|---|---|
| Sterile Water | WATER | Cardinal Health 107, LLC | 9655cd02-82b5-4a75-813b-854b19551481 | 2026-07-21 | Warnings, Adverse reactions | 059QF0KO0R |
| Yodo Salil | OINTMENT | Laboratorio Neo Farmaco del Ecuador Neofarmaco Cia. LTDA. | 56812625-7eab-6a25-e063-6294a90a23fe | 2026-07-20 | Warnings | 70FD1KFU70 |
| Prid | ICHTHAMMOL, CALCIUM SULFIDE, CALENDULA OFFICINALIS FLOWERING TOP, ARNICA MONTANA, ECHINACEA ANGUSTIFOLIA, SILICON DIOXIDE, SULFUR | Hyland's Inc. | 49689eeb-7790-07f1-e063-6294a90a2df2 | 2026-07-16 | Warnings | 70FD1KFU70 |
| Leg Cramps PM | OYSTER SHELL CALCIUM CARBONATE, CRUDE, CAUSTICUM, MATRICARIA RECUTITA, CINCHONA OFFICINALIS BARK, COPPER, LYCOPODIUM CLAVATUM SPORE, MAGNESIUM PHOSPHATE, DIBASIC TRIHYDRATE, TOXICODENDRON PUBESCENS LEAF, SILICON DIOXIDE, AND SULFUR | Hyland's Inc. | b0574a7e-88fa-417e-b6d5-60ced59eba47 | 2026-07-15 | Warnings | 2E32821G6I 70FD1KFU70 C88X29Y479 |
| EPINEPHRINE | EPINEPHRINE | Fresenius Kabi USA, LLC | 4f83895f-638c-4515-af03-7c41ae60a42e | 2026-07-15 | Warnings, Adverse reactions | YKH834O4BH |
| Acthar | REPOSITORY CORTICOTROPIN | Mallinckrodt ARD LLC | 7b48ddec-e815-45f4-9ca0-5c0daaf56f30 | 2026-07-15 | Warnings, Adverse reactions | K0U68Q2TXA |
| Sodium Sulfacetamide and Sulfur | SODIUM SULFACETAMIDE AND SULFUR | Acella Pharmaceuticals, LLC | c3ff4716-6009-4e29-9da9-ea740726cc3c | 2026-07-14 | Warnings, Adverse reactions | 70FD1KFU70 |
| Sodium Sulfacetamide 9 Sulfur 4.5 Wash | SULFACETAMIDE SODIUM AND SULFUR | Acella Pharmaceuticals, LLC | a761feea-86b6-44f0-8f9a-50d29ebb60e9 | 2026-07-14 | Warnings, Adverse reactions | 70FD1KFU70 |
| SODIUM SULFACETAMIDE - SULFUR WASH | SODIUM SULFACETAMIDE, SULFUR | ACELLA PHARMACEUTICALS | d9c5e993-e82a-436f-bd95-8984935c6551 | 2026-07-14 | Warnings, Adverse reactions | 70FD1KFU70 |
| Sodium Sulfacetamide 10 Sulfur 5 Cleanser | SULFACETAMIDE SODIUM AND SULFUR | Acella Pharmaceuticals, LLC | 1926eadd-d11f-44fa-971f-0041060f7589 | 2026-07-14 | Warnings, Adverse reactions | 70FD1KFU70 |
| SODIUM SULFACETAMIDE, SULFUR | SODIUM SULFACETAMIDE AND SULFUR | Acella Pharmaceuticals, LLC | 99705c54-b7af-423d-8f20-881e8fea236f | 2026-07-13 | Warnings, Adverse reactions | 70FD1KFU70 |
| Magnilife Eczema Care | SULFUR, GRAPHITE, DAPHNE MEZEREUM BARK, TOXICODENDRON PUBESCENS WHOLE | The Magni Group, Inc. | 8e3fc743-4c82-4a03-a963-2d5f93a1bc26 | 2026-07-13 | Warnings | 70FD1KFU70 |
| Sodium Sulfacetamide 10 Sulfur 2 cream | SULFACETAMIDE SODIUM AND SULFUR | Acella Pharmaceuticals, LLC | a57b734d-5d6d-4cd7-8003-9174cc785e41 | 2026-07-13 | Warnings, Adverse reactions | 70FD1KFU70 |
| Sodium Sulfacetamide 10 Sulfur 2 Cleanser | SULFACETAMIDE SODIUM AND SULFUR | Acella Pharmaceuticals, LLC | 210774a9-aaab-4bd4-ac5a-481ed72e0c0c | 2026-07-13 | Warnings, Adverse reactions | 70FD1KFU70 |
| Sodium Sulfacetamide 9.8% and Sulfur 4.8% Cleanser | SULFACETAMIDE SODIUM, SULFUR | Acella Pharmaceuticals, LLC | b21b36da-5475-4b01-8afd-1598f29c9b5d | 2026-07-13 | Warnings, Adverse reactions | 70FD1KFU70 |
| Epinephrine | EPINEPHRINE | A-S Medication Solutions | 6e811e28-0199-4df7-a916-5940c632401d | 2026-07-13 | Warnings, Adverse reactions | YKH834O4BH |
| EPINEPHRINE | EPINEPHRINE | CIVICA, INC. | 4a79ad00-405b-4454-a692-7f1daac4adec | 2026-07-10 | Warnings, Adverse reactions | YKH834O4BH |
| Freskaro Ear Drops for Swimmers | FRESKARO EAR DROPS FOR SWIMMERS | Pharma Nobis, LLC | 4f724d85-cd38-41da-e063-6394a90a9fd7 | 2026-07-08 | Warnings | PDC6A3C0OX |
| Nicomide | NIACINAMIDE, ZINC GLYCINATE, LEVOMEFOLATE CALCIUM, CUPRIC OXIDE, SELENIUM AND CHROMIUM | Avion Pharmaceuticals, LLC | 799b7705-4627-4c07-8d83-52b76290af9c | 2026-07-07 | Warnings | 25X51I8RD4 |
| Artificial Tears | ARTIFICIAL TEARS | AvPAK | f18bebf2-1936-658f-e053-2a95a90a5012 | 2026-07-07 | Warnings | PDC6A3C0OX |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.