Sunmark
- Product NDC
- 17856-0832
- 11-digit product format
- 178560832
- Labeler code
- 17856
- Product ID
- 17856-0832_5e547123-ad7f-41e8-8544-7103d7fe0ea9
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Mineral
- Dosage form
- OIL
- Route
- ORAL
- Labeler
- ATLANTIC BIOLOGICALS CORP.
- Application
- part334
- Marketing category
- OTC MONOGRAPH NOT FINAL
- Marketing start
- 2019-04-10
- Marketing end
- 0000-00-00
- Substance
- MINERAL OIL
- Active strength
- 999 mg/mL
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 17856-0832 | SUNMARK (MINERAL) OIL [ATLANTIC BIOLOGICALS CORP.] | 4 | Legacy NDC | 20240522_e95248fd-c26b-436c-bf62-b9c6790c2e91.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 17856-0832-1 | 17856083201 | 50 CUP, UNIT-DOSE in 1 BOX, UNIT-DOSE (17856-0832-1) > 30 mL in 1 CUP, UNIT-DOSE (17856-0832-2) | 2022-12-02 | 0000-00-00 | No | No | Current |