Orajel Denture Pain Relief
- Product NDC
- 10237-765
- 11-digit product format
- 102370765
- Labeler code
- 10237
- Product ID
- 10237-765_95318143-8df9-6885-e053-2a95a90a5277
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Benzocaine, Benzalkonium Chloride, Menthol
- Dosage form
- GEL
- Route
- TOPICAL
- Labeler
- Church & Dwight Co., Inc.
- Application
- part356
- Marketing category
- OTC MONOGRAPH NOT FINAL
- Marketing start
- 2016-07-01
- Marketing end
- 0000-00-00
- Substance
- MENTHOL; BENZOCAINE
- Active strength
- 26 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#