Acne Vanish Synergy

Product NDC
70470-1002
11-digit product format
704701002
Labeler code
70470
Product ID
70470-1002_9afb60b3-7d2e-2409-e053-2995a90a8603
Type
HUMAN OTC DRUG
Nonproprietary name
Acne Vanish
Dosage form
OIL
Route
TOPICAL
Labeler
PHYTOPIA CO., LTD.
Application
part356
Marketing category
OTC MONOGRAPH NOT FINAL
Marketing start
2016-02-29
Marketing end
0000-00-00
Substance
THYMOL
Active strength
1 g/50g
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
ebc62596-fc97-4d03-9483-7ba095d25db7Product name120151210

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
70470-1002-52021-01-29C16284748780-1ba0f9c33-5e7d-a910-e053-dadaa90a0b853fa059c8-0710-65a7-e054-00144ff8d46c

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
70470-1002-5Acne Vanish Synergyfor treatment of Acnes50 g in 1 BOTTLE, GLASSOIL502

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
70470-1002ACNE VANISH SYNERGY FOR TREATMENT OF ACNES (ACNE VANISH) OIL [PHYTOPIA CO., LTD.]2Legacy NDC, 1 package rows20191231_3fa059c8-0710-65a7-e054-00144ff8d46c.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsStatus
70470-1002-57047010020550 g in 1 BOTTLE, GLASS50 gHistorical