bu SPF 50 KIDS Broad Spectrum Alcohol-Free Performance Sunscreen - Fragrance Free

Product NDC
70325-5002
11-digit product format
703255002
Labeler code
70325
Product ID
70325-5002_3ee36a5c-108a-4f48-907c-4d8fb9372f34
Type
HUMAN OTC DRUG
Nonproprietary name
OCTINOXATE, OCTOCRYLENE, OCTISALATE, AVOBENZONE, and HOMOSALATE
Dosage form
SPRAY
Route
TOPICAL
Labeler
Bu Brands, LLC
Application
part352
Marketing category
OTC MONOGRAPH NOT FINAL
Marketing start
2016-12-01
Marketing end
0000-00-00
Substance
OCTINOXATE; OCTOCRYLENE; OCTISALATE; AVOBENZONE; HOMOSALATE
Active strength
8 g/100mL; g/100mL; g/100mL; g/100mL; g/100mL
NDC exclude flag
No
Listing certified through
2022-12-31
Current FDA listing
Historical FDA.report record

Reported adverse events (FAERS/openFDA)#

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

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
70325-5002-17032550020130 mL in 1 BOTTLE (70325-5002-1) 30 ml2016-12-010000-00-00NoNoCurrent
70325-5002-37032550020398 mL in 1 BOTTLE (70325-5002-3) 98 ml2016-12-010000-00-00NoNoCurrent