warnings
Warnings: If symptoms persist or worsen, or if pregnant or nursing, consult a doctor. Keep out of reach of children. Do not use if cap seal is broken or missing.
Acid Reflux 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
- Acid Reflux Relief
- Generic name
- CAPSICUM, SODIUM PHOSPHATE, DIBASIC, HEPTAHYDRATE, STRYCHNOS NUX-VOMICA SEED, ROBINIA PSEUDOACACIA BARK, SULFUR, SEPIA OFFICINALIS JUICE
- Manufacturer
- Homeocare Laboratories
- Product type
- HUMAN OTC DRUG
- SPL set ID
- 01ddf3ee-e925-404d-9b41-7876d5fd6634
- SPL ID
- 848ca4be-1f89-b274-e053-2a91aa0ad774
- Version
- 2
- Effective date
- 2019-03-20
- Source export date
- 2026-09-28
- Source partition
- 12
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0012-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-09-28/663999d0fe1757c1e2cd13a4799d76d875f663e0bc57701092264ebe7febfc18/drug-label-0012-of-0014.json.zip
- Source manifest SHA-256
- cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
- Import run
- 20260929T050834Z
- Imported at
- 2026-09-29 06:28:02
| Harmonized routes |
|---|
| SUBLINGUAL |
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 | Acid Reflux Relief | openfda.brand_name | |
| generic name | CAPSICUM, SODIUM PHOSPHATE, DIBASIC, HEPTAHYDRATE, STRYCHNOS NUX-VOMICA SEED, ROBINIA PSEUDOACACIA BARK, SULFUR, SEPIA OFFICINALIS JUICE | openfda.generic_name | |
| manufacturer name | Homeocare Laboratories | openfda.manufacturer_name | |
| ndc | package | 61727-331-21 | openfda.package_ndc |
| ndc | product | 61727-331 | openfda.product_ndc |
| ndc11 | package | 61727033121 | derived:openfda.package_ndc |
| spl id | 848ca4be-1f89-b274-e053-2a91aa0ad774 | id | |
| spl set id | 01ddf3ee-e925-404d-9b41-7876d5fd6634 | set_id | |
| unii | 00UK7646FG | openfda.unii | |
| unii | 269XH13919 | openfda.unii | |
| unii | QDL83WN8C2 | openfda.unii | |
| unii | 70FD1KFU70 | openfda.unii | |
| unii | 7TPC058OWY | openfda.unii | |
| unii | 70WT22SF4B | 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.