Petroleum

Product NDC
51143-069
11-digit product format
511430069
Labeler code
51143
Product ID
51143-069_bd80f13e-7320-45ac-acb4-375db38fb2ac
Type
HUMAN OTC DRUG
Nonproprietary name
White Petrolatum
Dosage form
JELLY
Route
TOPICAL
Labeler
Onpoint, Inc
Application
part347
Marketing category
OTC MONOGRAPH FINAL
Marketing start
2009-10-14
Marketing end
0000-00-00
Substance
PETROLATUM
Active strength
1 g/g
NDC exclude flag
No
Listing certified through
2021-12-31
Current FDA listing
Historical FDA.report record

NDC auxiliary status#

Explicit status records from FDA unfinished, excluded, and compounder auxiliary files. Absence of a row is not itself a regulatory status. Browse every current auxiliary row, including rows without a usable NDC. · Browse every captured source and parsed snapshot.

Current NDC status page 1 of 1 · 3 matching rows.

Dataset, Scope, Product NDC table
DatasetScopeProduct NDCPackage NDCCodeStatusReporting periodSource date
excluded productproduct51143-069DDiscontinued by firm2026-08-03
excluded packagepackage51143-06951143-069-27DDiscontinued by firm2026-08-03
excluded packagepackage51143-06951143-069-96DDiscontinued by firm2026-08-03

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
PETROLATUMACTIVE INGREDIENT4T6H12BN9UPETROLEUM (WHITE PETROLATUM) JELLY [ONPOINT, INC]2
PETROLATUMACTIVE MOIETY4T6H12BN9UPETROLEUM (WHITE PETROLATUM) JELLY [ONPOINT, INC]2