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Product NDC
49967-308
11-digit product format
499670308
Labeler code
49967
Product ID
49967-308_e87dfc45-39c8-4371-95b3-c27c1af923f1
Type
HUMAN OTC DRUG
Nonproprietary name
benzoyl peroxide
Dosage form
LIQUID
Route
TOPICAL
Labeler
L'Oreal USA Products Inc
Application
part333D
Marketing category
OTC MONOGRAPH FINAL
Marketing start
2017-08-10
Marketing end
0000-00-00
Substance
BENZOYL PEROXIDE
Active strength
25 mg/mL
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 NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
49967-308-0149967030801237 mL in 1 BOTTLE, PLASTIC (49967-308-01) 237 ml2017-08-100000-00-00NoNoCurrent
49967-308-024996703080259 mL in 1 BOTTLE, PLASTIC (49967-308-02) 59 ml2017-08-100000-00-00NoNoCurrent