Complete Beauty

Product NDC
0869-0503
11-digit product format
008690503
Labeler code
0869
Product ID
0869-0503_9a223f47-8b84-4c5a-96ae-cf6e526d57f7
Type
HUMAN OTC DRUG
Nonproprietary name
Octinoxate
Dosage form
LOTION
Route
TOPICAL
Labeler
Vi-Jon, LLC
Application
part352
Marketing category
OTC MONOGRAPH FINAL
Marketing start
2006-02-28
Marketing end
0000-00-00
Substance
OCTINOXATE; ZINC OXIDE
Active strength
60 mg/mL; mg/mL
NDC exclude flag
No
Listing certified through
2023-12-31
Current FDA listing
Historical FDA.report record

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionMarketing startMarketing endSampleExclude flagStatus
0869-0503-2600869050326118 BOTTLE, PUMP in 1 CARTON (0869-0503-26) > 118 mL in 1 BOTTLE, PUMP2006-02-280000-00-00NoNoCurrent
0869-0503-30008690503301 BOTTLE, PUMP in 1 CARTON (0869-0503-30) > 177 mL in 1 BOTTLE, PUMP2006-02-280000-00-00NoNoCurrent