Blemish Control Blotting Paper

Product NDC
76449-050
11-digit product format
764490050
Labeler code
76449
Product ID
76449-050_8d673888-8afe-4340-a182-05dfedc64ece
Type
HUMAN OTC DRUG
Nonproprietary name
Salicylic Acid
Dosage form
STRIP
Route
TOPICAL
Labeler
NYX Los Angeles Inc.
Application
part358H
Marketing category
OTC MONOGRAPH FINAL
Marketing start
2011-12-15
Marketing end
0000-00-00
Substance
SALICYLIC ACID
Active strength
0 mg/1
NDC exclude flag
E
Listing certified through
2017-12-31
Current FDA listing
Historical FDA.report record

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
dea2eded-d1e7-46bb-9a3d-f8dc20de6277Product name120190408

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
76449-050-012019-11-13C16284748780-197449f38-cd10-f6ea-e053-dbdaa90aa703Blemish Control Blotting Paper

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
76449-050-01Blemish Control Blotting Paper100 in 1 PACKAGESTRIP1004

DailyMed Socrata Ingredients#

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
76449-050BLEMISH CONTROL BLOTTING PAPER (SALICYLIC ACID) STRIP [NYX LOS ANGELES INC.]4Legacy NDC, 1 package rows20111215_26841133-310f-4799-b143-3972d8e83f9a.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionStatus
76449-050-0176449005001100 in 1 PACKAGEHistorical