Teatrical Pro-Aclarant Skin Lightening

Product NDC
50066-072
11-digit product format
500660072
Labeler code
50066
Product ID
50066-072_975473b0-1767-4756-9fab-bc36d38db0b5
Type
HUMAN OTC DRUG
Nonproprietary name
Hydroquinone
Dosage form
CREAM
Route
TOPICAL
Labeler
Genomma Lab USA
Application
part358A
Marketing category
OTC MONOGRAPH NOT FINAL
Marketing start
2020-04-22
Marketing end
0000-00-00
Substance
HYDROQUINONE
Active strength
20 mg/g
NDC exclude flag
No
Listing certified through
2021-12-31
Current FDA listing
Historical FDA.report record

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
85490a6b-2306-6bf2-c51b-eb63537dc2daProduct name120140508

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
50066-072-012022-01-28C16284748780-1d6a99b39-55d3-a426-e053-dadaa90af4c2Teatrical ® Pro-Aclarant Skin Lightening Cream

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
50066-072-01Teatrical Pro-Aclarant Skin Lightening48 g in 1 TUBECREAM481
50066-072-01Teatrical Pro-Aclarant Skin Lightening1 in 1 CARTONCREAM11

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
50066-072TEATRICAL PRO-ACLARANT SKIN LIGHTENING (HYDROQUINONE) CREAM [GENOMMA LAB USA]1Legacy NDC, 2 package rows20200423_c20869a0-1b14-4df5-aeab-ce9c85513141.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
50066-072-01500660072011 TUBE in 1 CARTON (50066-072-01) > 48 g in 1 TUBE1 tube2020-04-220000-00-00NoNoCurrent