Vitamin C Daily Moisturizer

Product NDC
62282-170
Requested package NDC
62282-170-01
11-digit product format
622820170
Labeler code
62282
Product ID
62282-170_eec7463c-2e87-73e0-e053-2a95a90a972f
Type
HUMAN OTC DRUG
Nonproprietary name
Octinoxate, Octisalate, Avobenzone, Octocrylene
Dosage form
LOTION
Route
TOPICAL
Labeler
Northwest Cosmetic Laboratories
Application
part352
Marketing category
OTC MONOGRAPH NOT FINAL
Marketing start
2010-06-01
Marketing end
0000-00-00
Substance
AVOBENZONE; OCTINOXATE; OCTISALATE; OCTOCRYLENE
Active strength
2 g/100mL; g/100mL; g/100mL; g/100mL
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.

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
62282-170-016228201700150 mL in 1 TUBE (62282-170-01) 50 ml2010-06-010000-00-00NoNoCurrent