Genesis Sensitive Fresh Mint

Product NDC
71771-001
11-digit product format
717710001
Labeler code
71771
Product ID
71771-001_5a41534d-e77e-e4ac-e053-2a91aa0afa8a
Type
HUMAN OTC DRUG
Nonproprietary name
POTASSIUM NITRATE, SODIUM FLUORIDE
Dosage form
PASTE
Route
DENTAL
Labeler
Dr Bobs Inc
Application
part356
Marketing category
OTC MONOGRAPH NOT FINAL
Marketing start
2017-09-28
Marketing end
0000-00-00
Substance
POTASSIUM NITRATE; SODIUM FLUORIDE
Active strength
50 mg/g; mg/g
NDC exclude flag
E
Listing certified through
2018-12-31
Current FDA listing
Historical FDA.report record

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
71771-001-002020-02-03C16284748780-19d75b9d0-33be-f424-e053-dadaa90a57cee72979ac-b7d0-49a6-ab5d-3248621a9ad9
71771-001-002020-01-31C16284748780-19d75b9d0-33be-f424-e053-dadaa90a57cee72979ac-b7d0-49a6-ab5d-3248621a9ad9