warnings
Warnings Stop use and ask a doctor if ■ pain gets worse or lasts more than 7 days. ■ new symptoms occur. ■ redness or swelling is present If pregnant or breastfeeding Ask a health professional before use. Keep out of reach of children.
Backache Relief
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
- Backache Relief
- Generic name
- ACONITUM NAPELLUS, BRYONIA ALBA ROOT, MAGNESIUM PHOSPHATE, DIBASIC TRIHYDRATE, BELLIS PERENNIS, TOXICODENDRON PUBESCENS LEAF AND ARNICA MONTANA
- Manufacturer
- Hyland's Inc.
- Product type
- HUMAN OTC DRUG
- SPL set ID
- a51452b3-0aba-6928-e053-2995a90a1619
- SPL ID
- fb5962be-5af1-206f-e053-6294a90aa8b0
- Version
- 4
- Effective date
- 2023-05-10
- Source export date
- 2026-09-28
- Source partition
- 2
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0002-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-09-28/f7d2b6e3f8600cd856280ab55a9c6fa54a642647191d164f9d1110e89f3f4097/drug-label-0002-of-0014.json.zip
- Source manifest SHA-256
- cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
- Import run
- 20260929T050834Z
- Imported at
- 2026-09-29 05:15:20
| 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 | Backache Relief | openfda.brand_name | |
| generic name | ACONITUM NAPELLUS, BRYONIA ALBA ROOT, MAGNESIUM PHOSPHATE, DIBASIC TRIHYDRATE, BELLIS PERENNIS, TOXICODENDRON PUBESCENS LEAF AND ARNICA MONTANA | openfda.generic_name | |
| manufacturer name | Hyland's Inc. | openfda.manufacturer_name | |
| ndc | package | 54973-4011-1 | openfda.package_ndc |
| ndc | product | 54973-4011 | openfda.product_ndc |
| ndc11 | package | 54973401101 | derived:openfda.package_ndc |
| spl id | fb5962be-5af1-206f-e053-6294a90aa8b0 | id | |
| spl set id | a51452b3-0aba-6928-e053-2995a90a1619 | set_id | |
| unii | O80TY208ZW | openfda.unii | |
| unii | 2HU33I03UY | openfda.unii | |
| unii | HF539G9L3Q | openfda.unii | |
| unii | 6IO182RP7A | openfda.unii | |
| unii | T7J046YI2B | openfda.unii | |
| unii | U0NQ8555JD | 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.