Softlips Oasis Strawberry Kiwi

Product NDC
10742-8746
11-digit product format
107428746
Labeler code
10742
Product ID
10742-8746_08ef87ac-fa34-487b-9cf9-b7c4ba4b95d0
Type
HUMAN OTC DRUG
Nonproprietary name
dimethicone, oxybenzone, octinoxate
Dosage form
STICK
Route
TOPICAL
Labeler
The Mentholatum Company
Application
part352
Marketing category
OTC MONOGRAPH FINAL
Marketing start
2019-05-01
Marketing end
0000-00-00
Substance
DIMETHICONE; OCTINOXATE; OXYBENZONE
Active strength
20 mg/g; mg/g; mg/g
NDC exclude flag
No
Listing certified through
2020-12-31
Current FDA listing
Historical FDA.report record

FDA-Initiated Inactive NDC Indexing#

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
10742-8746-1107428746011 TUBE in 1 BLISTER PACK (10742-8746-1) > 4.5 g in 1 TUBE1 tube2019-05-010000-00-00NoNoCurrent
10742-8746-2107428746024.5 g in 1 TUBE (10742-8746-2) 4.5 g2019-07-150000-00-00NoNoCurrent