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Product NDC
70512-200
11-digit product format
705120200
Labeler code
70512
Product ID
70512-200_a6b7dc1d-caaa-7e4f-e053-2995a90a0c44
Type
HUMAN OTC DRUG
Nonproprietary name
menthol liquid
Dosage form
LIQUID
Route
TOPICAL
Labeler
Sola Pharmaceuticals
Application
part348
Marketing category
OTC MONOGRAPH NOT FINAL
Marketing start
2020-05-28
Marketing end
0000-00-00
Substance
MENTHOL
Active strength
30 mg/mL
NDC exclude flag
No
Listing certified through
2021-12-31
Current FDA listing
Historical FDA.report record

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
70512-200-902022-12-05C16284748780-1d6a99b39-f3b0-a426-e053-dadaa90af4c2a6b7dc1d-caa9-7e4f-e053-2995a90a0c44
70512-200-902022-01-28C16284748780-1d6a99b39-f3b0-a426-e053-dadaa90af4c2a6b7dc1d-caa9-7e4f-e053-2995a90a0c44

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
70512-200-907051202009088.7 mL in 1 BOTTLE (70512-200-90) 88.7 ml2020-05-280000-00-00NoNoCurrent