Gaviscon
- Product NDC
- 0135-0430
- 11-digit product format
- 001350430
- Labeler code
- 0135
- Product ID
- 0135-0430_02f611d3-df31-4514-86ae-9e81004acdbf
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- aluminum hydroxide and magnesium carbonate
- Dosage form
- TABLET, CHEWABLE
- Route
- ORAL
- Labeler
- Haleon US Holdings LLC
- Application
- M001
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2011-06-13
- Substance
- ALUMINUM HYDROXIDE; MAGNESIUM CARBONATE
- Active strength
- 160; 105 mg/1; mg/1
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Observed NDC auxiliary status history#
This history shows the information present in each captured FDA auxiliary file. It is not a continuous regulatory timeline, and a missing record does not establish a status.
| Captured / source date | Dataset | Scope | Package NDC | Code | Status | Snapshot | Source SHA-256 |
|---|---|---|---|---|---|---|---|
| 2025-02-02 03:52 UTC · source 2025-01-31 | excluded product | product | U | Excluded because listing certification expired | 302b2466d912… | e7b80fea0513… | |
| 2025-02-02 03:52 UTC · source 2025-01-31 | excluded package | package | 0135-0430-03 | U | Excluded because listing certification expired | 302b2466d912… | e7b80fea0513… |
| 2025-01-20 13:05 UTC · source 2025-01-20 | excluded product | product | U | Excluded because listing certification expired | ed331223b511… | 672a5bd82f5f… | |
| 2025-01-20 13:05 UTC · source 2025-01-20 | excluded package | package | 0135-0430-03 | U | Excluded because listing certification expired | ed331223b511… | 672a5bd82f5f… |
| 2025-01-11 03:41 UTC · source 2025-01-10 | excluded product | product | U | Excluded because listing certification expired | 0efc9e666f02… | f202fb6c5f17… | |
| 2025-01-11 03:41 UTC · source 2025-01-10 | excluded package | package | 0135-0430-03 | U | Excluded because listing certification expired | 0efc9e666f02… | f202fb6c5f17… |
| 2022-08-30 03:57 UTC · source 2022-08-29 | excluded product | product | I | Inactivated by FDA | fb8cb913e6d1… | eb8c232b6be0… | |
| 2022-08-30 03:57 UTC · source 2022-08-29 | excluded package | package | 0135-0430-03 | I | Inactivated by FDA | fb8cb913e6d1… | eb8c232b6be0… |
| 2020-06-10 20:45 UTC · source 2020-06-10 | excluded product | product | I | Inactivated by FDA | 9bebd1f3094a… | 5416666fcb17… | |
| 2020-06-10 20:45 UTC · source 2020-06-10 | excluded package | package | 0135-0430-03 | I | Inactivated by FDA | 9bebd1f3094a… | 5416666fcb17… |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Gaviscon
- Brand name suffix
- Extra Strength
- Listing expiration
- 2026-12-31
Active Ingredients#
| Ingredient | Strength |
|---|---|
| ALUMINUM HYDROXIDE | 160 mg/1 |
| MAGNESIUM CARBONATE | 105 mg/1 |
Harmonized UNII identifiers#
| Identifier | FDA.report destination |
|---|---|
| 5QB0T2IUN0 | Internal UNII lookup |
| 0E53J927NA | Internal UNII lookup |
Harmonized RxCUI identifiers#
Harmonized SPL set identifiers#
| Identifier | FDA.report destination |
|---|---|
| 7f367927-c366-465c-a059-e2cfb337d562 | Available on FDA.report |
DailyMed Product Concepts#
| Product concept | Relation | Version | Effective |
|---|---|---|---|
| fb7ab793-2c12-4079-b100-a64f73bef25a | Product name | 4 | 20240712 |
| b0cbf770-6cc3-4aa4-9158-755110c2b9f7 | Product name | 2 | 20230717 |
| dc7c5daa-021f-40dd-b00d-63982cb2067a | Product name | 1 | 20230426 |
| 08ffbcbf-26df-b99c-1dab-64fc4cfae89f | Product name | 5 | 20200925 |
| 816b97af-edc5-4060-aff1-b814bdbcad50 | Product name | 1 | 20190415 |
| 7cda52fc-125f-421c-8fea-bc1974370c49 | Product name | 2 | 20180703 |
| 419aab54-5d5a-4146-9453-026d4a9991be | Product name | 2 | 20170525 |
| 08ffbcbf-26df-b99c-1dab-64fc4cfae89f | Product name | 2 | 20160823 |
| 89dac932-b90a-4410-9ab1-84c53e57de25 | Product name | 1 | 20150316 |
FDA-Initiated Inactive NDC Indexing#
| Effective | Related label |
|---|---|
| 2025-02-01 | Drug Facts |
| 2023-04-18 | Drug Facts |
| 2022-07-29 | Drug Facts |
| 2020-11-18 | Drug Facts |
| 2020-01-31 | Drug Facts |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 0135-0430-03 | GavisconExtra Strength | 100 in 1 BOTTLE | TABLET, CHEWABLE | 100 | 17 |
DailyMed Billing Units#
| Package NDC | Billing unit | Product NDC | DailyMed indexing SPL | SPL version | Effective |
|---|---|---|---|---|---|
| 0135-0430-03 | EA - Each | 0135-0430 | 909107f4-1ed7-4afe-a965-cdc166c28a1c | 1 | 2012-07-24 |
DailyMed Socrata Ingredients#
DailyMed Dashboard NDC Coverage#
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 0135-0430 | GAVISCON EXTRA STRENGTH (ALUMINUM HYDROXIDE AND MAGNESIUM CARBONATE) TABLET, CHEWABLE GAVISCON REGULAR STRENGTH (ALUMINUM HYDROXIDE AND MAGNESIUM TRISILICATE) TABLET, CHEWABLE [HALEON US HOLDINGS LLC] | 16 | Current NDC, Legacy NDC, 1 package rows | 20250516_7f367927-c366-465c-a059-e2cfb337d562.zip |
openFDA label cross-check#
OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.
| Brand | Generic | Manufacturer | SPL set ID | Effective date | Available safety fields | Join |
|---|---|---|---|---|---|---|
| FEVIA Acid Control | CALCIUM CARBONATE | VIVUNT PHARMA LLC | 4d695a90-6502-3020-e063-6394a90ab0c3 | 2026-07-15 | Warnings | M001 |
| GOOD NEIGHBOR PHARMACY Antacid Extra Strength | ALUMINUM HYDROXIDE AND MAGNESIUM CARBONATE | Amerisource Bergen | 5e346dc0-69ce-4cc5-bb5d-bfa833e11c1f | 2026-07-13 | Warnings | M001 |
| Major Regular Strength Assorted Flavors | ANTACID TABLETS | Major Pharmaceuticals | 2ba0eeb2-7048-4259-83d5-9f4ec1c92d32 | 2026-07-13 | Warnings | M001 |
| Good Neighbor Extra Strength Assorted Fruits | CALCIUM CARBONATE | AMERISOURCE BERGEN | abf564a1-0823-433d-a023-8be4e085daf4 | 2026-07-13 | Warnings | M001 |
| Omeprazole, 24/7 Life by 7-Eleven | OMEPRAZOLE TABLET, DELAYED RELEASE | Lil' Drug Store Products, Inc. | 36d8a272-6cca-e759-e063-6394a90a9df8 | 2026-07-08 | Warnings | M001 |
| Tums Ultra | CALCIUM CARBONATE | Haleon US Holdings LLC | c544120f-15f0-48b5-88b2-d4820f180f50 | 2026-07-07 | Warnings | M001 |
| Regular Strength Assorted Flavors | ANTACID CALCIUM CARBONATE | AKRON PHARMA INC | 3f7fe022-aee9-b899-e063-6394a90afb4e | 2026-07-07 | Warnings | M001 |
| Magnesium Oxide | MAGNESIUM OXIDE | Westminster Pharmaceuticals, LLC | 52eeac0e-94bb-48c3-81dc-578e96406c01 | 2026-07-06 | Warnings | M001 |
| Kids Tummy Relief | CALCIUM CARBONATE | PNP Pharmaceuticals Inc. | 5103a317-5c4a-ec96-e063-6294a90aad7e | 2026-07-01 | Warnings | M001 |
| Childrens Antacid | CALCIUM CARBONATE | DOLGENCORP, LLC | 4d6ebc7e-ef39-47e8-91e9-f38484329fa9 | 2026-06-30 | Warnings | M001 |
| Ultra Strength Antacid | CALCIUM CARBONATE CHEWABLE TABLETS | CVS Pharmacy. Inc. | 24cec2bc-cf12-b513-e063-6394a90a9447 | 2026-06-30 | Warnings | M001 |
| Childrens Stomach Relief | CALCIUM CARBONATE | Chain Drug Marketing Association, Inc. | fb47d693-72d7-4586-9855-5e833ad1406f | 2026-06-18 | Warnings | M001 |
| Dr. Sana Alivio Digestivo UPSET STOMACH | EFEFERVESCENT ANTACID | EVI LABS | 51b8750c-3fcf-2543-e063-6394a90a7a8f | 2026-06-16 | Warnings | M001 |
| E-Z-GAS II | ANTACID/ANTIFLATULENT | E-Z-EM, INC. | 4e12e1cb-b033-076d-e054-00144ff8d46c | 2026-06-15 | Warnings | M001 |
| Sodium Bicarbonate | SODIUM BICARBONATE | Cardinal Health 107, LLC | 60c2a176-8854-4479-b853-d07fe9a1830c | 2026-06-12 | Warnings | M001 |
| Mag-Al Plus | ALUMINUM HYDROXIDE, MAGNESIUM HYDROXIDE, AND SIMETHICONE | Cardinal Health 107, LLC | 08df7403-9ee3-4a43-a151-c1a6ef7a7549 | 2026-06-10 | Warnings | M001 |
| Childrens Antacid | CALCIUM CARBONATE | Rite Aid Corporation | d09c2d99-9a1f-4eae-a048-ab6dbf74a798 | 2026-06-09 | Warnings | M001 |
| Maximum Strength Calcium Carbonate 1000mg | CALCIUM CARBONATE CHEWABLE TABLETS | CVS HEALTH CORP | 24ce4597-b571-3cbf-e063-6394a90a8ea2 | 2026-06-09 | Warnings | M001 |
| Tums Chewy Bites with Gas Relief | CALCIUM CARBONATE AND SIMETHICONE | Haleon US Holdings LLC | 6d7be7e4-4bff-4cfd-bbbe-df412ac9db10 | 2026-06-09 | Warnings | M001 |
| Sodium Bicarbonate Antacid | SODIUM BICARBONATE | NCS HealthCare of KY, LLC dba Vangard Labs | fde4ea0c-152b-4b79-a6d8-2b0dbd9107aa | 2026-06-04 | Warnings | M001 |
DailyMed RxNorm Mappings#
| RxCUI | RxNorm string | TTY | DailyMed | SPL version |
|---|---|---|---|---|
| 308072 | aluminum hydroxide 160 MG / magnesium carbonate 105 MG Chewable Tablet | PSN | 7f367927-c366-465c-a059-e2cfb337d562 | 17 |
| 212978 | Gaviscon Extra Strength 160 MG / 105 MG Chewable Tablet | PSN | 7f367927-c366-465c-a059-e2cfb337d562 | 17 |
| 212978 | aluminum hydroxide 160 MG / magnesium carbonate 105 MG Chewable Tablet [Gaviscon] | SBD | 7f367927-c366-465c-a059-e2cfb337d562 | 17 |
| 308072 | aluminum hydroxide 160 MG / magnesium carbonate 105 MG Chewable Tablet | SCD | 7f367927-c366-465c-a059-e2cfb337d562 | 17 |
| 212978 | Gaviscon Extra Strength (aluminum hydroxide 160 MG / magnesium carbonate 105 MG) Chewable Tablet | SY | 7f367927-c366-465c-a059-e2cfb337d562 | 17 |
Packages#
| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|---|---|---|---|---|---|---|
| 0135-0430-03 | 00135043003 | 100 TABLET, CHEWABLE in 1 BOTTLE (0135-0430-03) | 2011-06-13 | 0000-00-00 | No | No | Current |