Home NDC 17856-1831 Oil
Product NDC 17856-1831
11-digit product format 178561831
Labeler code 17856
Product ID 17856-1831_5a821986-f187-540a-e063-6394a90ac67e
Type HUMAN OTC DRUG
Nonproprietary name Mineral Oil
Dosage form OIL
Route ORAL
Labeler Atlantic Biologicals Corp.
Application M007
Marketing category OTC MONOGRAPH DRUG
Marketing start 1989-07-15
Substance MINERAL OIL
Active strength 1 mg/mL
NDC exclude flag No
Listing certified through 2027-12-31
Current FDA listing Yes Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.
Additional Listing Data#
Finished product Yes
Brand name base Oil
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength MINERAL OIL 1 mg/mL
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination T5L8T28FGP Internal UNII lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
openFDA label cross-check# OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.
Matched openFDA labels page 14 of 42 · 833 matching rows.
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Marketing start Sample Exclude flag Status 17856-1831-5 17856183105 50 CUP, UNIT-DOSE in 1 CASE (17856-1831-5) / 30 mL in 1 CUP, UNIT-DOSE 2026-09-02 No No Current 17856-1831-8 17856183108 48 CUP, UNIT-DOSE in 1 CASE (17856-1831-8) / 30 mL in 1 CUP, UNIT-DOSE 2026-09-02 No No Current