No-Ad Sun Care

Product NDC
58443-0229
11-digit product format
584430229
Labeler code
58443
Product ID
58443-0229_9c5a1bf7-5b31-67b8-e053-2a95a90a903c
Type
HUMAN OTC DRUG
Nonproprietary name
Avobenzone, homosalate, octisalate, and oxybenzone
Dosage form
LOTION
Route
TOPICAL
Labeler
Prime Enterprises Inc.
Application
part352
Marketing category
OTC MONOGRAPH FINAL
Marketing start
2016-04-06
Marketing end
0000-00-00
Substance
OXYBENZONE; AVOBENZONE; HOMOSALATE; OCTISALATE
Active strength
30 mg/mL; mg/mL; mg/mL; mg/mL
NDC exclude flag
No
Listing certified through
2021-12-31
Current FDA listing
Historical FDA.report record

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
58443-0229-658443022906475 mL in 1 BOTTLE (58443-0229-6) 475 ml2016-04-060000-00-00NoNoCurrent