Pharmacys Prescription 8 OZ Acne Control

Product NDC
72197-015
11-digit product format
721970015
Labeler code
72197
Product ID
72197-015_914a2512-8a3b-7771-e053-2a95a90a72e3
Type
HUMAN OTC DRUG
Nonproprietary name
Salicylic Acid
Dosage form
LIQUID
Route
TOPICAL
Labeler
American Consumer Products Corp
Application
part333D
Marketing category
OTC MONOGRAPH FINAL
Marketing start
2019-09-16
Marketing end
0000-00-00
Substance
SALICYLIC ACID
Active strength
0 g/100mL
NDC exclude flag
No
Listing certified through
2020-12-31
Current FDA listing
Historical FDA.report record

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
d5e51f11-ad28-caa4-4b49-4143974782adProduct name120150831

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
72197-015-082023-01-30C16284748780-1f386c649-a5fe-0266-e053-dadaa90a7c1aPharmacys Prescription 8 OZ Acne Control

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
72197-015-08Pharmacys Prescription 8 OZ Acne Control236.58 mL in 1 BOTTLELIQUID236.581

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
72197-015PHARMACYS PRESCRIPTION 8 OZ ACNE CONTROL (SALICYLIC ACID) LIQUID [AMERICAN CONSUMER PRODUCTS CORP]1Legacy NDC, 1 package rows20190917_914a2512-8a3a-7771-e053-2a95a90a72e3.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
72197-015-0872197001508236.58 mL in 1 BOTTLE (72197-015-08) 236.58 ml2019-09-160000-00-00NoNoCurrent