Home NDC 83079-002 Good Instincts Proper Sunscreen SPF 50
Product NDC 83079-002
11-digit product format 830790002
Labeler code 83079
Product ID 83079-002_54dd9438-b225-f3e4-e063-6394a90a8c02
Type HUMAN OTC DRUG
Nonproprietary name ZINC OXIDE, TITANIUM DIOXIDE
Dosage form CREAM
Route TOPICAL
Labeler Inhabit Brands, Inc
Application M020
Marketing category OTC MONOGRAPH DRUG
Marketing start 2026-04-01
Substance ZINC OXIDE; TITANIUM DIOXIDE
Active strength 221; 37 mg/mL; mg/mL
Pharmacologic classes Copper Absorption Inhibitor [EPC], Decreased Copper Ion Absorption [PE]
NDC exclude flag No
Listing certified through 2027-12-31
Current FDA listing Yes Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.
Additional Listing Data#
Finished product Yes
Brand name base Good Instincts Proper Sunscreen SPF 50
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength ZINC OXIDE 221 mg/mL TITANIUM DIOXIDE 37 mg/mL
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 2 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination SOI2LOH54Z Internal UNII lookup 15FIX9V2JP Internal UNII lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
openFDA label cross-check# OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.
Matched openFDA labels page 45 of 357 · 7,139 matching rows.
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Sample Exclude flag Status 83079-002-01 83079000201 1 TUBE in 1 BOX (83079-002-01) / 10 mL in 1 TUBE 1 tube 2026-04-01 No No Current