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

NDC auxiliary status#

These records are reproduced from FDA’s unfinished, excluded, and compounder listings. They describe what appeared in the source files; a missing record does not establish a regulatory status. View all current auxiliary records, including entries without an NDC. · View the auxiliary file history.

Current NDC status page 1 of 1 · 2 matching rows.

Dataset, Scope, Product NDC table
DatasetScopeProduct NDCPackage NDCCodeStatusReporting periodSource date
excluded productproduct17856-0832DDiscontinued by firm2026-08-11
excluded packagepackage17856-083217856-0832-1DDiscontinued by firm2026-08-11

Observed NDC auxiliary status history#

This history shows the information present in each captured FDA auxiliary file. It is not a continuous regulatory timeline, and a missing record does not establish a status.

Historic NDC status page 1 of 1 · 8 matching rows.

View current auxiliary records. · View the auxiliary file history.

Captured / source date, Dataset, Scope table
Captured / source dateDatasetScopePackage NDCCodeStatusSnapshotSource SHA-256
2025-12-14 17:58 UTC · source 2025-12-05excluded productproductDDiscontinued by firmd630ba8d3edf…732f749b63fb…
2025-12-14 17:58 UTC · source 2025-12-05excluded packagepackage17856-0832-1DDiscontinued by firmd630ba8d3edf…732f749b63fb…
2025-08-27 00:01 UTC · source 2025-08-26excluded productproductDDiscontinued by firmf5e01cc5f278…a2eaf40c39c3…
2025-08-27 00:01 UTC · source 2025-08-26excluded packagepackage17856-0832-1DDiscontinued by firmf5e01cc5f278…a2eaf40c39c3…
2024-05-15 03:39 UTC · source 2024-05-14excluded productproductIInactivated by FDA834df4deac94…adcc014656a3…
2024-05-15 03:39 UTC · source 2024-05-14excluded packagepackage17856-0832-1IInactivated by FDA834df4deac94…adcc014656a3…
2024-03-11 06:39 UTC · source 2024-03-08excluded productproductIInactivated by FDA1332a3947898…d4bfe170f9cd…
2024-03-11 06:39 UTC · source 2024-03-08excluded packagepackage17856-0832-1IInactivated by FDA1332a3947898…d4bfe170f9cd…

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
17856-0832-12024-05-20C16284748780-11030e365-2f2c-111a-e063-dadaa90a10e2Mineral Oil
17856-0832-12024-01-30C16284748780-11030e365-2f2c-111a-e063-dadaa90a10e2Mineral Oil

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
17856-0832SUNMARK (MINERAL) OIL [ATLANTIC BIOLOGICALS CORP.]4Legacy NDC20240522_e95248fd-c26b-436c-bf62-b9c6790c2e91.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionMarketing startMarketing endSampleExclude flagStatus
17856-0832-11785608320150 CUP, UNIT-DOSE in 1 BOX, UNIT-DOSE (17856-0832-1) > 30 mL in 1 CUP, UNIT-DOSE (17856-0832-2) 2022-12-020000-00-00NoNoCurrent