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
- 2026-10-30
- 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/2026-10-30/9abf0f8b126f8aad070e21ea702bfb5e39ce670b16ae57dd52e8877705d1bf5d/drug-label-0011-of-0014.json.zip
- Source manifest SHA-256
- b11f1f6b476c7417db937215bf14307ef1a0b69465b42b411ad52f42ae36ead3
- Import run
- 20261102T182004Z
- Imported at
- 2026-11-02 19:29:49
| 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.