Aim Sensitive

Product NDC
10237-632
11-digit product format
102370632
Labeler code
10237
Product ID
10237-632_9376e043-f45a-5c1f-e053-2a95a90ac1ce
Type
HUMAN OTC DRUG
Nonproprietary name
Potassium nitrate, Sodium Fluoride
Dosage form
GEL, DENTIFRICE
Route
DENTAL
Labeler
Church & Dwight Co., Inc.
Application
part356
Marketing category
OTC MONOGRAPH NOT FINAL
Marketing start
2015-03-25
Marketing end
0000-00-00
Substance
POTASSIUM NITRATE; SODIUM FLUORIDE
Active strength
50 mg/g; mg/g
NDC exclude flag
No
Listing certified through
2020-12-31
Current FDA listing
Historical FDA.report record

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
10237-632-552024-06-14C16284748780-1ba0f9c33-1ef2-a910-e053-dadaa90a0b851222bc2f-6e77-6cbc-e054-00144ff8d46c
10237-632-552021-01-29C16284748780-1ba0f9c33-1ef2-a910-e053-dadaa90a0b851222bc2f-6e77-6cbc-e054-00144ff8d46c