NDC 49035-101-01 - equate Ultra Strength Antacid Peppermint Flavor
This NDC is not currently matched to an FDA NDC product listing in FDA.report, but it is a valid NDC-form code. FDA.report is showing the available DailyMed label context for the product root.
- Product NDC
- 49035-101
- Requested NDC
- 49035-101-01
- Package NDCs from labels
- 49035-101-47, 49035-101-01, 49035-101-02
- Manufacturer
- Wal-Mart Stores,Inc.,
- Effective date
- 2025-10-27
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Antacid Tablets - Wal-Mart Stores,Inc., | Wal-Mart Stores,Inc., | 2025-10-27 | HUMAN OTC DRUG LABEL |
| Cherry Blossom Hand Sanitizer | Wal-Mart Stores, Inc. | 2011-04-11 | HUMAN OTC DRUG LABEL |
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 49035-101-47 | equate Ultra Strength AntacidPeppermint Flavor | 160 in 1 BOTTLE, PLASTIC | TABLET, CHEWABLE | 160 | 7 | |
| 49035-101-01 | Hand Sanitizer Bodycology | 30 mL in 1 BOTTLE | GEL | 30 | 3 | |
| 49035-101-02 | Hand Sanitizer Bodycology | 1 in 1 BOTTLE | GEL | 1 | 3 |
DailyMed Dashboard NDC Coverage#
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 49035-101 | EQUATE ULTRA STRENGTH ANTACID PEPPERMINT FLAVOR (ANTACID TABLETS) TABLET, CHEWABLE [WAL-MART STORES,INC.,] | 6 | Current NDC, Legacy NDC, 1 package rows | 20241116_6a18cd92-cc51-401b-9074-fbaa1afb42ac.zip |
| 49035-101 | HAND SANITIZER (ETHYL ALCOHOL) GEL [WAL-MART STORES, INC.] | 3 | Current NDC, Legacy NDC, 2 package rows | 20110413_3ca632ea-6404-4d91-bffc-7162aecb0ce5.zip |
DailyMed Socrata Ingredients#
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.
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.