MD ACNE Customized treatment

Product NDC
71804-852
11-digit product format
718040852
Labeler code
71804
Product ID
71804-852_5b5a74a5-b52f-0776-e053-2991aa0ab5b2
Type
HUMAN OTC DRUG
Nonproprietary name
BENZOYL PEROXIDE
Dosage form
CREAM
Route
TOPICAL
Labeler
MDalgorithms Inc
Application
part333D
Marketing category
OTC MONOGRAPH FINAL
Marketing start
2017-10-12
Marketing end
0000-00-00
Substance
BENZOYL PEROXIDE
Active strength
50 mg/mL
NDC exclude flag
No
Listing certified through
2020-12-31
Current FDA listing
Historical FDA.report record

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
71804-852-007180408520090 mL in 1 TUBE (71804-852-00) 90 ml2017-10-120000-00-00NoNoCurrent