Ultra V IDEBENONE SKINFIT CUSHION

Product NDC
71975-060
11-digit product format
719750060
Labeler code
71975
Product ID
71975-060_3e7a3b08-a763-400f-bad8-8b0a2d9d7d7a
Type
HUMAN OTC DRUG
Nonproprietary name
Titanium Dioxide, Octinoxate, Zinc Oxide
Dosage form
POWDER
Route
TOPICAL
Labeler
Ultra V Co., Ltd
Application
part352
Marketing category
OTC MONOGRAPH NOT FINAL
Marketing start
2018-01-02
Marketing end
0000-00-00
Substance
TITANIUM DIOXIDE; OCTINOXATE; ZINC OXIDE
Active strength
1 g/14g; g/14g; g/14g
NDC exclude flag
No
Listing certified through
2020-12-31
Current FDA listing
Historical FDA.report record

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
71975-060-022023-06-08C16284748780-1f386c649-ef71-0266-e053-dadaa90a7c1a8c0f4ba9-2744-4712-81e2-8a20acbba16c
71975-060-022023-01-30C16284748780-1f386c649-ef71-0266-e053-dadaa90a7c1a8c0f4ba9-2744-4712-81e2-8a20acbba16c

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
71975-060-02719750060021 CONTAINER in 1 CARTON (71975-060-02) > 14 g in 1 CONTAINER (71975-060-01) 1 container2018-01-020000-00-00NoNoCurrent