Pre and Post Sx Pouch

Product NDC
53225-5000
11-digit product format
532255000
Labeler code
53225
Product ID
53225-5000_cdc81943-00f1-5460-e053-2995a90a1311
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Mupirocin 2%, Dimethicone 5%, Chlorhexidine Gluconate 4%
Dosage form
KIT
Route
TOPICAL
Labeler
Terrain Pharmaceuticals
Marketing category
UNAPPROVED DRUG OTHER
Marketing start
2018-01-19
Marketing end
0000-00-00
Active strength
0
NDC exclude flag
No
Listing certified through
2022-12-31
Current FDA listing
Historical FDA.report record

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
53225-5000-1EA - Each53225-5000be26bbb4-abb7-4906-b3e7-99ac05f5712912018-02-20

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
53225-5000-1532255000011 KIT in 1 KIT (53225-5000-1) * 1 TUBE in 1 CARTON (45802-112-22) > 22 g in 1 TUBE * 118 mL in 1 TUBE (53329-151-04) * 118 mL in 1 BOTTLE, PLASTIC (0116-1061-04) 1 kit2018-01-190000-00-00NoNoCurrent