BABY GUM RELIEF
- Product NDC
- 59262-502
- 11-digit product format
- 592620502
- Labeler code
- 59262
- Product ID
- 59262-502_b0b8413d-2d5b-4e27-a213-5573dd1e3e0d
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- CALCIUM FLUORIDE, CHAMOMILE, FERRUM PHOSPHORICUM, OYSTER SHELL CALCIUM CARBONATE, CRUDE, PODOPHYLLUM and TRIBASIC CALCIUM PHOSPHATE
- Dosage form
- TABLET, ORALLY DISINTEGRATING
- Route
- ORAL
- Labeler
- Similasan Corporation
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start
- 2018-06-15
- Marketing end
- 0000-00-00
- Substance
- OYSTER SHELL CALCIUM CARBONATE, CRUDE; CALCIUM FLUORIDE; TRIBASIC CALCIUM PHOSPHATE; CHAMOMILE; FERROSOFERRIC PHOSPHATE; PODOPHYLLUM
- Active strength
- 12 [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1
- NDC exclude flag
- No
- Listing certified through
- 2019-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Product Concepts#
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 59262-502-26 | BABY GUM RELIEF | 1 in 1 BOX | TABLET, ORALLY DISINTEGRATING | 1 | | 2 |
| 59262-502-26 | BABY GUM RELIEF | 135 in 1 BOTTLE | TABLET, ORALLY DISINTEGRATING | 135 | | 2 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 59262-502 | BABY GUM RELIEF (CALCIUM FLUORIDE, CHAMOMILE, FERRUM PHOSPHORICUM, OYSTER SHELL CALCIUM CARBONATE, CRUDE, PODOPHYLLUM AND TRIBASIC CALCIUM PHOSPHATE) TABLET, ORALLY DISINTEGRATING [SIMILASAN CORPORATION] | 2 | Legacy NDC, 2 package rows | 20180906_5d49e61d-7bd1-4211-bbad-80da9d7dfabf.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Status |
|---|
| 59262-502-26 | 59262050226 | 1 in 1 BOX | Historical |