Home NDC 53225-5000
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 Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Marketing end Sample Exclude flag Status 53225-5000-1 53225500001 1 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 kit 2018-01-19 0000-00-00 No No Current