SUNZONE FAMILY SUNSCREEN SPF 30

Product NDC
50021-144
11-digit product format
500210144
Labeler code
50021
Product ID
50021-144_38676290-f5ea-470f-bf1c-7c4fce8b059d
Type
HUMAN OTC DRUG
Nonproprietary name
Octinoxate, Octocrylene, Octisalate, Oxybenzone, Avobenzone and Homosalate.
Dosage form
AEROSOL, SPRAY
Route
TOPICAL
Labeler
Empack Spraytech Inc.
Application
part352
Marketing category
OTC MONOGRAPH NOT FINAL
Marketing start
2012-11-08
Marketing end
0000-00-00
Substance
OCTINOXATE; OCTOCRYLENE; OCTISALATE; OXYBENZONE; AVOBENZONE; HOMOSALATE
Active strength
11 g/153g; g/153g; g/153g; g/153g; g/153g; g/153g
NDC exclude flag
E
Listing certified through
2017-12-31
Current FDA listing
Historical FDA.report record

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
50021-144-012025-02-10C16284748780-19855d018-e2eb-cd31-e053-dbdaa90ab51a6e0659a8-e7f0-4398-8599-7112c392b5fb
50021-144-012019-11-27C16284748780-19855d018-e2eb-cd31-e053-dbdaa90ab51a6e0659a8-e7f0-4398-8599-7112c392b5fb