SUNSCREEN

Product NDC
51414-905
11-digit product format
514140905
Labeler code
51414
Product ID
51414-905_da8b7c91-74fb-3c9b-e053-2995a90ac715
Type
HUMAN OTC DRUG
Nonproprietary name
Octinoxate,ZINC OXIDE,OCTISALATE
Dosage form
STICK
Route
TOPICAL
Labeler
Yuyao Jessie Commodity Co.,Ltd.
Application
part352
Marketing category
OTC MONOGRAPH NOT FINAL
Marketing start
2014-05-08
Marketing end
0000-00-00
Substance
OCTINOXATE; OCTISALATE; ZINC OXIDE
Active strength
3 g/100g; g/100g; g/100g
Pharmacologic classes
Copper Absorption Inhibitor [EPC], Decreased Copper Ion Absorption [PE]
NDC exclude flag
No
Listing certified through
2023-12-31
Current FDA listing
Historical FDA.report record

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.

FDA-Initiated Inactive NDC Indexing#

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
51414-905-015141409050110 g in 1 PACKAGE (51414-905-01) 10 g2018-01-050000-00-00NoNoCurrent
51414-905-025141409050213 g in 1 PACKAGE (51414-905-02) 13 g2018-01-050000-00-00NoNoCurrent
51414-905-035141409050314 g in 1 PACKAGE (51414-905-03) 14 g2018-01-050000-00-00NoNoCurrent
51414-905-045141409050415 g in 1 PACKAGE (51414-905-04) 15 g2018-01-050000-00-00NoNoCurrent
51414-905-055141409050516 g in 1 PACKAGE (51414-905-05) 16 g2018-01-050000-00-00NoNoCurrent
51414-905-065141409050619 g in 1 PACKAGE (51414-905-06) 19 g2018-01-050000-00-00NoNoCurrent
51414-905-075141409050720 g in 1 PACKAGE (51414-905-07) 20 g2018-01-050000-00-00NoNoCurrent
51414-905-085141409050825 g in 1 PACKAGE (51414-905-08) 25 g2018-01-050000-00-00NoNoCurrent
51414-905-095141409050930 g in 1 PACKAGE (51414-905-09) 30 g2018-01-050000-00-00NoNoCurrent
51414-905-10514140905102 g in 1 PACKAGE (51414-905-10) 2 g2018-01-050000-00-00NoNoCurrent