Paulas Choice Extra Care Non-Greasy Sunscreen SPF 50

Product NDC
76144-232
11-digit product format
761440232
Labeler code
76144
Product ID
76144-232_c54df1c4-712c-bc46-e053-2995a90ab473
Type
HUMAN OTC DRUG
Nonproprietary name
Homosalate, Oxybenzone, Octisalate, Avobenzone, Octocrylene
Dosage form
LOTION
Route
TOPICAL
Labeler
Paula's Choice, LLC
Application
part352
Marketing category
OTC MONOGRAPH NOT FINAL
Marketing start
2008-08-07
Marketing end
0000-00-00
Substance
OCTISALATE; OCTOCRYLENE; OXYBENZONE; HOMOSALATE; AVOBENZONE
Active strength
50 mg/mL; mg/mL; mg/mL; mg/mL; mg/mL
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#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
76144-232-002020-01-31C16284748780-19d75b9d1-291f-f424-e053-dadaa90a57ce1e11867f-8964-6253-e054-00144ff88e88
76144-232-092020-01-31C16284748780-19d75b9d1-291f-f424-e053-dadaa90a57ce1e11867f-8964-6253-e054-00144ff88e88

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
76144-232-0176144023201148 mL in 1 TUBE (76144-232-01) 148 ml2008-08-070000-00-00NoNoCurrent
76144-232-03761440232033.5 mL in 1 PACKET (76144-232-03) 3.5 ml2008-08-070000-00-00NoNoCurrent