Publix Ultra Strength
- Product NDC
- 41415-103
- 11-digit product format
- 414150103
- Labeler code
- 41415
- Product ID
- 41415-103_4235b220-b979-0210-e063-6394a90a45db
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Calcium Carbonate
- Dosage form
- TABLET, CHEWABLE
- Route
- ORAL
- Labeler
- PUBLIX SUPER MARKETS, INC
- Application
- M001
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2019-05-21
- 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
- Publix Ultra Strength
- Brand name suffix
- Assorted Fruit
- 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 |
|---|
| 41415-103-72 | Publix Ultra StrengthAssorted Fruit | 72 in 1 BOTTLE, PLASTIC | TABLET, CHEWABLE | 72 | | 7 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 41415-103 | PUBLIX ULTRA STRENGTH ASSORTED FRUIT (CALCIUM CARBONATE) TABLET, CHEWABLE [PUBLIX SUPER MARKETS, INC] | 6 | Current NDC, Legacy NDC, 1 package rows | 20241030_9e1c883f-016e-4c05-b27a-750d14c0f3e5.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 |
|---|
| 41415-103-72 | 41415010372 | 72 TABLET, CHEWABLE in 1 BOTTLE, PLASTIC (41415-103-72) | 2019-05-21 | 0000-00-00 | No | No | Current |