warnings
WARNINGS In case of overdose, get medical help or contact a poison control center right away. Keep out of the reach of children. If pregnant or breastfeeding, ask a healthcare professional before use.
Cellular Oxygenator Drops 2095
openFDA label record#
This page contains supplementary openFDA label data. For the canonical label presentation, use the corresponding DailyMed Structured Product Label.
Verified complete openFDA source JSON
- Brand name
- Cellular Oxygenator Drops 2095
- Generic name
- CELLULAR OXYGENATOR DROPS
- Manufacturer
- Professional Complementary Health Formulas
- Product type
- HUMAN OTC DRUG
- SPL set ID
- 5aba4627-6078-4c9e-93ee-690cfe3439cf
- SPL ID
- 7cd73e4a-7077-40ed-952f-a6f3094d26ea
- Version
- 2
- Effective date
- 2026-01-08
- Source export date
- 2026-11-06
- Source partition
- 10
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0010-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-11-06/b0d9ca61dc485ebaf55e14a76d7d677668e40ef1e1978cdbcc4d73d58eba0b99/drug-label-0010-of-0014.json.zip
- Source manifest SHA-256
- 4a7570ba105b5a039a8e1c94a85e7f085b9047a8882a35a96bf1e4516c5ffc97
- Import run
- 20261108T063105Z
- Imported at
- 2026-11-08 07:46:15
| Harmonized routes |
|---|
| ORAL |
Harmonized identifier links#
Every typed identifier imported from the complete openFDA harmonization object is paginated here; values are not reduced to a first match.
| Type | Scope | Identifier | Source field |
|---|---|---|---|
| brand name | Cellular Oxygenator Drops 2095 | openfda.brand_name | |
| generic name | CELLULAR OXYGENATOR DROPS | openfda.generic_name | |
| manufacturer name | Professional Complementary Health Formulas | openfda.manufacturer_name | |
| ndc | package | 63083-2095-2 | openfda.package_ndc |
| ndc | product | 63083-2095 | openfda.product_ndc |
| ndc11 | package | 63083209502 | derived:openfda.package_ndc |
| spl id | 7cd73e4a-7077-40ed-952f-a6f3094d26ea | id | |
| spl set id | 5aba4627-6078-4c9e-93ee-690cfe3439cf | set_id | |
| unii | 25X51I8RD4 | openfda.unii | |
| unii | T42NAD2KHC | openfda.unii | |
| unii | TLM2976OFR | openfda.unii | |
| unii | SAA04E81UX | openfda.unii | |
| unii | 73Y7P0K73Y | openfda.unii | |
| unii | HF539G9L3Q | openfda.unii | |
| unii | 3T006GV98U | openfda.unii | |
| unii | 8L70Q75FXE | openfda.unii | |
| unii | PQ6CK8PD0R | openfda.unii | |
| unii | 0U46U6E8UK | openfda.unii | |
| unii | 030MS0JBDO | openfda.unii | |
| unii | ZZ4AG7L7VM | openfda.unii | |
| unii | KV2JZ1BI6Z | openfda.unii | |
| unii | X66NSO3N35 | openfda.unii | |
| unii | 7114SV0MYK | openfda.unii |
Warnings cross-check#
openFDA text is shown for search and cross-checking; DailyMed SPL is canonical.
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.