MAXIMUM STRENGTH ANTACID CHERRY
- Product NDC
- 69842-683
- 11-digit product format
- 698420683
- Labeler code
- 69842
- Product ID
- 69842-683_7d77cd37-2ecf-d03c-e053-2a91aa0a7218
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- aluminum hydroxide, magnesium hydroxide, simethicone
- Dosage form
- SUSPENSION
- Route
- ORAL
- Labeler
- CVS
- Application
- part331
- Marketing category
- OTC MONOGRAPH FINAL
- Marketing start
- 2018-02-01
- Marketing end
- 0000-00-00
- Substance
- ALUMINUM HYDROXIDE; MAGNESIUM HYDROXIDE; DIMETHICONE
- Active strength
- 400 mg/5mL; mg/5mL; mg/5mL
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- Current FDA listing
- Historical FDA.report record
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 69842-683-12 | MAXIMUM STRENGTH ANTACID CHERRY | 355 mL in 1 BOTTLE | SUSPENSION | 355 | | 3 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 69842-683 | MAXIMUM STRENGTH ANTACID CHERRY (ALUMINUM HYDROXIDE, MAGNESIUM HYDROXIDE, SIMETHICONE) SUSPENSION [CVS] | 3 | Legacy NDC, 1 package rows | 20241208_7d77c710-bfe1-0722-e053-2991aa0a2eea.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 69842-683-12 | 69842068312 | 355 mL in 1 BOTTLE (69842-683-12) | 355 ml | 2018-02-01 | 0000-00-00 | No | No | Current |