Ultra Strength Assorted Fruit Antacid
- Product NDC
- 42507-709
- 11-digit product format
- 425070709
- Labeler code
- 42507
- Product ID
- 42507-709_1b9efee7-3f3f-410c-8308-213068644f6e
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Calcium carbonate
- Dosage form
- TABLET, CHEWABLE
- Route
- ORAL
- Labeler
- Hyvee Inc
- Application
- M001
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2026-03-26
- Substance
- CALCIUM CARBONATE
- Active strength
- 1000 mg/1
- Pharmacologic classes
- Blood Coagulation Factor [EPC], Calcium [CS], Cations, Divalent [CS], Increased Coagulation Factor Activity [PE], Phosphate Binder [EPC], Phosphate Chelating Activity [MoA]
- NDC exclude flag
- No
- Listing certified through
- 2027-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Ultra Strength Assorted Fruit Antacid
- Listing expiration
- 2027-12-31
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 |
|---|
| 42507-709-68 | Ultra Strength Assorted Fruit Antacid | 72 in 1 BOTTLE | TABLET, CHEWABLE | 72 | | 2 |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Sample | Exclude flag | Status |
|---|
| 42507-709-68 | 42507070968 | 72 TABLET, CHEWABLE in 1 BOTTLE (42507-709-68) | 2026-03-26 | No | No | Current |