Home NDC 11701-048 Baza Clear
Product NDC 11701-048
11-digit product format 117010048
Labeler code 11701
Product ID 11701-048_f9da667f-f66e-432a-9f43-3520193da004
Type HUMAN OTC DRUG
Nonproprietary name Petrolatum
Dosage form OINTMENT
Route TOPICAL
Labeler Coloplast Corp
Application M016
Marketing category OTC MONOGRAPH DRUG
Marketing start 2009-06-15
Substance PETROLATUM
Active strength 960 mg/g
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 Baza Clear
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength PETROLATUM 960 mg/g
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 4T6H12BN9U Internal UNII lookup
Harmonized RxCUI identifiers# RxCUI identifiers page 1 of 1 · 2 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 686454 Internal RxNorm lookup 1085651 Internal RxNorm lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
FDA-Initiated Inactive NDC Indexing# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 11701-048-14 Baza Clear 142 g in 1 TUBE OINTMENT 142 7 11701-048-22 Baza Clear 4 g in 1 PACKET OINTMENT 4 7 11701-048-24 Baza Clear 50 g in 1 TUBE OINTMENT 50 7
DailyMed Socrata Ingredients# DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 11701-048 BAZA CLEAR (PETROLATUM) OINTMENT [COLOPLAST MANUFACTURING US, LLC] 6 Current NDC, Legacy NDC, 3 package rows 20231222_69d9f456-1a35-4146-8366-c0285648a172.zip
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 39 of 68 · 1,357 matching rows.
DailyMed RxNorm Mappings# Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Marketing end Sample Exclude flag Status 11701-048-14 11701004814 142 g in 1 TUBE (11701-048-14) 142 g 2009-06-15 0000-00-00 No No Current 11701-048-22 11701004822 4 g in 1 PACKET (11701-048-22) 4 g 2009-06-15 0000-00-00 No No Current 11701-048-24 11701004824 50 g in 1 TUBE (11701-048-24) 50 g 2009-06-15 0000-00-00 No No Current