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Product NDC
43596-0875
11-digit product format
435960875
Labeler code
43596
Product ID
43596-0875_aa553db9-db23-44e8-e053-2a95a90a3388
Type
HUMAN OTC DRUG
Nonproprietary name
Octinoxate, Zinc Oxide
Dosage form
CREAM
Route
TOPICAL
Labeler
Ventura Corporation LTD
Application
part352
Marketing category
OTC MONOGRAPH FINAL
Marketing start
2020-04-01
Marketing end
0000-00-00
Substance
OCTINOXATE; ZINC OXIDE
Active strength
4 g/100g; g/100g
NDC exclude flag
No
Listing certified through
2021-12-31
Current FDA listing
Historical FDA.report record

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
43596-0875-12025-04-22C16284748780-1d6a99b39-681d-a426-e053-dadaa90af4c2a4628b10-fc80-1b15-e053-2a95a90a2958
43596-0875-12022-01-28C16284748780-1d6a99b39-681d-a426-e053-dadaa90af4c2a4628b10-fc80-1b15-e053-2a95a90a2958

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
43596-0875-14359608750130 g in 1 TUBE (43596-0875-1) 30 g2020-04-010000-00-00NoNoCurrent