warnings
WARNINGS Do not take more than 15 mL (age 2-5 yrs) or 30 mL (age 6-11 yrs) in a 24-hour period, or use the maximum dosage of this product for more than 2 weeks, except under the advice and supervision of a doctor.
Childrens Stomach Relief Antacid
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
- Childrens Stomach Relief Antacid
- Generic name
- CALCIUM CARBONATE
- Manufacturer
- H E B
- Product type
- HUMAN OTC DRUG
- SPL set ID
- 18fae1aa-1001-8035-e063-6394a90adc66
- SPL ID
- e6b41a8d-5bad-42bc-9de0-8262d04f170a
- Version
- 2
- Effective date
- 2025-01-14
- Source export date
- 2026-10-12
- Source partition
- 1
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0001-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-10-12/7928c8e8c6256620071a8b7e5b93eb8dfa543649c08d17a01ea02251012ba58c/drug-label-0001-of-0014.json.zip
- Source manifest SHA-256
- 7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
- Import run
- 20261013T011858Z
- Imported at
- 2026-10-13 01:25:16
| 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 |
|---|---|---|---|
| application number | M001 | openfda.application_number | |
| brand name | Childrens Stomach Relief Antacid | openfda.brand_name | |
| generic name | CALCIUM CARBONATE | openfda.generic_name | |
| manufacturer name | H E B | openfda.manufacturer_name | |
| ndc | package | 37808-638-03 | openfda.package_ndc |
| ndc | product | 37808-638 | openfda.product_ndc |
| ndc11 | package | 37808063803 | derived:openfda.package_ndc |
| rxcui | 308901 | openfda.rxcui | |
| spl id | e6b41a8d-5bad-42bc-9de0-8262d04f170a | id | |
| spl set id | 18fae1aa-1001-8035-e063-6394a90adc66 | set_id | |
| unii | H0G9379FGK | 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.