FDA.reportPublic FDA data

NeoBenz Micro Plus Pack

Product NDC
67402-021
11-digit product format
674020021
Labeler code
67402
Product ID
67402-021_827f05fc-94d5-4bde-8c2f-e97d250d9660
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
benzoyl peroxide
Dosage form
KIT
Labeler
SkinMedica Pharmaceuticals, Inc.
Marketing category
UNAPPROVED DRUG OTHER
Marketing start
2009-04-16
NDC exclude flag
No
Current FDA listing
Yes

Additional Listing Data#

Finished product
Yes
Brand name base
NeoBenz Micro Plus Pack

Harmonized SPL set identifiers#

SPL set identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
bb5a8842-7fdd-404f-815d-c0d0714e1db8Not currently hydrated or indexed on FDA.report

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
67402-021-23EA - Each67402-021b2748b97-8580-41dd-9c0c-fed92dbb27ba12012-07-24

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 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
NeoBenz Micro Plus PackBENZOYL PEROXIDESkinMedica Pharmaceuticals, Inc.bb5a8842-7fdd-404f-815d-c0d0714e1db82010-05-12Warnings, Adverse reactionsExact identifier
ndc (product): 67402-021

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
67402-021-23674020021231 KIT in 1 BOX (67402-021-23) * 7 POUCH in 1 CASE (67402-023-07) / .5 g in 1 POUCH (67402-023-01) * 45 g in 1 TUBE1 kit2009-04-160000-00-00NoNoCurrent