warnings
Warning For external use only. Do not use on: Deep or puncture wounds Animal bites Serious burns When using this product: Do not get into eyes or mucous membranes.
OWELL NATURALS DRAW MAX
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
- OWELL NATURALS DRAW MAX
- Generic name
- APIS MELLIFICA, CALENDULA OFFICINALIS, ECHINACEA PURPUREA, HEPAR SULPHURIS CALCAREUM, LEDUM PALUSTRE, URTICA DIOICA
- Manufacturer
- OWELL NATURALS LLC
- Product type
- HUMAN OTC DRUG
- SPL set ID
- 57b30ce7-31c3-ed55-e063-6294a90a68f3
- SPL ID
- 57b30ce7-31c4-ed55-e063-6294a90a68f3
- Version
- 1
- Effective date
- 2026-07-28
- Source export date
- 2026-09-28
- Source partition
- 11
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0011-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-09-28/aa96b5a2be6b394393acd0090f6948bdf99e0e8e00666f81608929c8fa83db77/drug-label-0011-of-0014.json.zip
- Source manifest SHA-256
- cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
- Import run
- 20260929T050834Z
- Imported at
- 2026-09-29 06:18:23
| Harmonized routes |
|---|
| TOPICAL |
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 | OWELL NATURALS DRAW MAX | openfda.brand_name | |
| generic name | APIS MELLIFICA, CALENDULA OFFICINALIS, ECHINACEA PURPUREA, HEPAR SULPHURIS CALCAREUM, LEDUM PALUSTRE, URTICA DIOICA | openfda.generic_name | |
| manufacturer name | OWELL NATURALS LLC | openfda.manufacturer_name | |
| ndc | package | 83570-009-01 | openfda.package_ndc |
| ndc | package | 83570-009-02 | openfda.package_ndc |
| ndc | product | 83570-009 | openfda.product_ndc |
| ndc11 | package | 83570000901 | derived:openfda.package_ndc |
| ndc11 | package | 83570000902 | derived:openfda.package_ndc |
| spl id | 57b30ce7-31c4-ed55-e063-6294a90a68f3 | id | |
| spl set id | 57b30ce7-31c3-ed55-e063-6294a90a68f3 | set_id | |
| unii | 877L01IZ0P | openfda.unii | |
| unii | 710FLW4U46 | openfda.unii | |
| unii | 18E7415PXQ | openfda.unii | |
| unii | QI7G114Y98 | openfda.unii | |
| unii | 7S82P3R43Z | openfda.unii | |
| unii | 1MBW07J51Q | 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.