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 |
|---|---|---|---|---|---|---|
| Antacid- Calcium Carbonate | CALCIUM CARBONATE | Anhui Jiuhe Health Industry Co., Ltd | 53518897-5387-38cf-e063-6394a90aa3e1 | 2026-06-02 | Warnings | M001 |
| ACID GONE ANTACID | ALUMINUM HYDROXIDE AND MAGNESIUM CARBONATE | Major Pharmaceuticals | 3d353a92-92f1-4304-8895-31d39dccd88c | 2026-06-01 | Warnings | M001 |
| Regular Strength Antacid Peppermint | CALCIUM CARBONATE | Hyvee Inc | 4e5526a8-d9ad-965b-e063-6294a90a8333 | 2026-06-01 | Warnings | M001 |
| REGULAR STRENGTH ANTACID/ANTIGAS | ALUMINUM HYDROXIDE, MAGNESIUM HYDROXIDE, DIMETHICONE | NuCare Pharmaceuticals, Inc. | 52e75fe4-f04f-31da-e063-6294a90a1e4f | 2026-05-28 | Warnings | M001 |
| Humco Sodium Bicarbonate | SODIUM BICARBONATE | Humco Holding Group, Inc. | aeaa34f6-216d-49f3-8393-c7bda96a3e32 | 2026-05-26 | Warnings | M001 |
| Magnesium Oxide | MAGNESIUM OXIDE | Bryant Ranch Prepack | 9875ae6b-2d91-49a3-9512-60a2b8bbccda | 2026-05-22 | Warnings | M001 |
| Regular Strength Antacid Assorted Fruit Regular strength Antacid | CALCIUM CARBONATE | Hyvee Inc | 4df2a8ee-c823-7a59-e063-6394a90ac556 | 2026-05-19 | Warnings | M001 |
| Extra Strength Antacid Assorted Fruit | CALCIUM CARBONATE | Hyvee Inc | 4cda1c1a-f5ff-5b77-e063-6294a90ad664 | 2026-05-13 | Warnings | M001 |
| Sodium Bicarbonate | SODIUM BICARBONATE | Vitamex USA, Corp | 5195cab5-bdda-2ddf-e063-6394a90ac9fe | 2026-05-11 | Warnings | M001 |
| Kesin MAG-AL Plus | ALUMINUM AND MAGNESIUM HYDROXIDE W/SIMETHICONE SUSPENSION | Kesin Pharma Corporation | 436b622a-f028-df98-e063-6394a90a3eaa | 2026-05-08 | Warnings | M001 |
| Kesin MAG-AL Plus XS | ALUMINUM AND MAGNESIUM HYDROXIDE W/SIMETHICONE SUSPENSION | Kesin Pharma Corporation | 436b89f7-e417-0df2-e063-6394a90a96df | 2026-05-08 | Warnings | M001 |
| Kesin MAG-AL | ALUMINUM AND MAGNESIUM HYDROXIDE SUSPENSION | Kesin Pharma Corporation | 42df2198-14dc-da1c-e063-6394a90a1ae6 | 2026-05-08 | Warnings | M001 |
| Supreme Antacid Cherry | CALCIUM CARBONATE, MAGNESIUM HYDROXIDE | CVS | 2bc4ad16-57a1-b585-e063-6394a90a5726 | 2026-05-07 | Warnings | M001 |
| GERI-LANTA ANTACID ANTIGAS | ALUMINUM HYDROXIDE, MAGNESIUM HYDROXIDE, DIMETHICONE | Preferred Pharmaceuticals Inc. | 27848ae0-3b2f-4bfe-8856-4b8de419091e | 2026-05-06 | Warnings | M001 |
| REGULAR STRENGTH ANTACID | ALUMINUM HYDROXIDE, MAGNESIUM HYDROXIDE, DIMETHICONE | Preferred Pharmaceuticals Inc. | ad3e7ebe-f2a9-4305-b370-59785f5396c8 | 2026-05-06 | Warnings | M001 |
| Leader Extra Strength Antacid | CALCIUM CARBONATE | CARDINAL HEALTH 110, LLC. DBA LEADER | c7a8c877-3e20-4910-8ea4-1714fac3ff2f | 2026-05-04 | Warnings | M001 |
| Sodium Bicarbonate | SODIUM BICARBONATE | TWIN MED LLC | 0f867f56-4bc0-4a85-b9d2-a16282b7c82b | 2026-05-01 | Warnings | M001 |
| Extra strength gas relief | SIMETHICONE | KROGER COMPANY | ea1c7b4c-91a1-0c1c-e053-2995a90ab823 | 2026-04-29 | Warnings | M001 |
| Calcium Carbonate | CALCIUM CARBONATE | Cardinal Health 107, LLC | 8109dd2b-875c-40eb-82ac-d3780bc0c437 | 2026-04-27 | Warnings | M001 |
| Magnesium Oxide | MAGNESIUM OXIDE | Bryant Ranch Prepack | 77fa8fe5-33ac-44b2-9596-5b276e9f2162 | 2026-04-24 | 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 |