Maximum Strength Medicated Foot Powder

Product NDC
11673-510
11-digit product format
116730510
Labeler code
11673
Product ID
11673-510_c77bfe32-c8a3-38e6-e053-2995a90ac3dd
Type
HUMAN OTC DRUG
Nonproprietary name
Medicated Foot Powder
Dosage form
POWDER
Route
TOPICAL
Labeler
Target Corporation
Application
part348
Marketing category
OTC MONOGRAPH NOT FINAL
Marketing start
2013-04-30
Marketing end
0000-00-00
Substance
MENTHOL
Active strength
0 g/g
NDC exclude flag
No
Listing certified through
2022-12-31
Current FDA listing
Historical FDA.report record

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
11673-510-102023-01-30C16284748780-1e4f33bdf-a654-d8a0-e053-dadaa90a6e4e444934d5-fe57-4ac2-be43-703b80a6d785
11673-510-102022-07-29C16284748780-1e4f33bdf-a654-d8a0-e053-dadaa90a6e4e444934d5-fe57-4ac2-be43-703b80a6d785

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
11673-510-1011673051010283 g in 1 BOTTLE, PLASTIC (11673-510-10) 283 g2013-04-300000-00-00NoNoCurrent