BEEVENOM SUN

Product NDC
51346-023
11-digit product format
513460023
Labeler code
51346
Product ID
51346-023_0efafa1c-d52b-4d45-920c-cbae86f5b1ee
Type
HUMAN OTC DRUG
Nonproprietary name
OCTINOXATE, TITANIUM DIOXIDE, OCTISALATE
Dosage form
CREAM
Route
TOPICAL
Labeler
NATURE REPUBLIC CO., LTD.
Application
part352
Marketing category
OTC MONOGRAPH FINAL
Marketing start
2012-02-01
Marketing end
0000-00-00
Substance
OCTINOXATE; TITANIUM DIOXIDE; OCTISALATE
Active strength
4 g/50mL; g/50mL; g/50mL
NDC exclude flag
E
Listing certified through
2018-12-31
Current FDA listing
Historical FDA.report record

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
51346-023-012021-07-10C16284748780-19d75b9d0-6b53-f424-e053-dadaa90a57cedd37bced-ebb7-412e-9aee-8e4df3644f70
51346-023-012020-01-31C16284748780-19d75b9d0-6b53-f424-e053-dadaa90a57cedd37bced-ebb7-412e-9aee-8e4df3644f70