ultra strength antacid
- Product NDC
- 11673-813
- 11-digit product format
- 116730813
- Labeler code
- 11673
- Product ID
- 11673-813_42c22d07-2b8a-a3c3-e063-6394a90a687a
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Calciium carbonate
- Dosage form
- TABLET, CHEWABLE
- Route
- ORAL
- Labeler
- Target Corporation
- Application
- M001
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2018-03-15
- Substance
- CALCIUM CARBONATE
- Active strength
- 1000 mg/1
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- ultra strength antacid
- Brand name suffix
- Peppermint Flavored
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| CALCIUM CARBONATE | 1000 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | H0G9379FGK |
| Rxcui | 308892 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 11673-813-47 | ultra strength antacidPeppermint Flavored | 160 in 1 BOTTLE, PLASTIC | TABLET, CHEWABLE | 160 | | 8 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 11673-813 | ULTRA STRENGTH ANTACID PEPPERMINT FLAVORED (CALCIIUM CARBONATE) TABLET, CHEWABLE [TARGET CORPORATION] | 7 | Current NDC, Legacy NDC, 1 package rows | 20241109_55dc1614-8fc0-4f2c-abfc-b675173b4f07.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 11673-813-47 | 11673081347 | 160 TABLET, CHEWABLE in 1 BOTTLE, PLASTIC (11673-813-47) | 2018-03-15 | 0000-00-00 | No | No | Current |