SPF Rx - Mineral Sunscreen SPF 30

Product NDC
55628-8569
11-digit product format
556288569
Labeler code
55628
Product ID
55628-8569_79e6154c-02f5-4d74-a7c6-bf937e5848a8
Type
HUMAN OTC DRUG
Nonproprietary name
Zinc Oxide, Titanium Dioxide
Dosage form
CREAM
Route
TOPICAL
Labeler
Cal Pharma LLC
Application
part352
Marketing category
OTC MONOGRAPH NOT FINAL
Marketing start
2017-07-30
Marketing end
0000-00-00
Substance
ZINC OXIDE; TITANIUM DIOXIDE
Active strength
5 g/100g; g/100g
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
55628-8569-42024-03-28C16284748780-1d6a99b39-cffa-a426-e053-dadaa90af4c299053ff8-2e52-4c14-b5f8-49957f910a70
55628-8569-42022-01-28C16284748780-1d6a99b39-cffa-a426-e053-dadaa90af4c299053ff8-2e52-4c14-b5f8-49957f910a70

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
55628-8569-455628856904120 g in 1 TUBE (55628-8569-4) 120 g2017-07-300000-00-00NoNoCurrent