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.
Low Back Pain Drops 2041
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
- Low Back Pain Drops 2041
- Generic name
- LOW BACK PAIN DROPS
- Manufacturer
- Professional Complementary Health Formulas
- Product type
- HUMAN OTC DRUG
- SPL set ID
- c9b3e606-5991-4ce4-9e0d-51bcb44da583
- SPL ID
- c9c4d3b5-15e8-4c7c-963a-4a2c76dc048b
- Version
- 2
- Effective date
- 2026-01-08
- Source export date
- 2026-10-12
- Source partition
- 7
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0007-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-10-12/ff22b88bd32e56cbc369af80345075227138a42b1b3ba9a84f038fd5493a7a47/drug-label-0007-of-0014.json.zip
- Source manifest SHA-256
- 7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
- Import run
- 20261013T011858Z
- Imported at
- 2026-10-13 01:59:32
| 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 | Low Back Pain Drops 2041 | openfda.brand_name | |
| generic name | LOW BACK PAIN DROPS | openfda.generic_name | |
| manufacturer name | Professional Complementary Health Formulas | openfda.manufacturer_name | |
| ndc | package | 63083-2041-2 | openfda.package_ndc |
| ndc | product | 63083-2041 | openfda.product_ndc |
| ndc11 | package | 63083204102 | derived:openfda.package_ndc |
| spl id | c9c4d3b5-15e8-4c7c-963a-4a2c76dc048b | id | |
| spl set id | c9b3e606-5991-4ce4-9e0d-51bcb44da583 | set_id | |
| unii | XK4IUX8MNB | openfda.unii | |
| unii | DD5FO1WKFU | openfda.unii | |
| unii | O80TY208ZW | openfda.unii | |
| unii | 4QQN74LH4O | openfda.unii | |
| unii | 1TH8Q20J0U | openfda.unii | |
| unii | QDL83WN8C2 | openfda.unii | |
| unii | HF539G9L3Q | openfda.unii | |
| unii | N1R7LRU866 | openfda.unii | |
| unii | 6IO182RP7A | openfda.unii | |
| unii | 7C0697DR9I | openfda.unii | |
| unii | S6G2NLH4Y7 | openfda.unii | |
| unii | U0NQ8555JD | openfda.unii | |
| unii | T4423S18FM | openfda.unii | |
| unii | 7S82P3R43Z | openfda.unii | |
| unii | 08X0K2M57P | openfda.unii | |
| unii | 11B89M58UN | openfda.unii | |
| unii | C88X29Y479 | 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.