First Mark
- Product NDC
- 51042-692
- 11-digit product format
- 510420692
- Labeler code
- 51042
- Product ID
- 51042-692_c6037bb7-6e78-4058-88eb-92c8290d092f
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Benzethonium Chloride
- Dosage form
- LIQUID
- Route
- TOPICAL
- Labeler
- Performance Food Group
- Application
- part333E
- Marketing category
- OTC MONOGRAPH NOT FINAL
- Marketing start
- 2010-06-23
- Marketing end
- 0000-00-00
- Substance
- BENZETHONIUM CHLORIDE
- Active strength
- 0 mg/100mL
- 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 | Document | Indexing SPL | Related label |
|---|---|---|---|---|---|
| 51042-692-17 | 2023-07-25 | C162847 | 48780-1 | 956f9ecf-d803-621f-e053-dbdaa90a74ad | 51260354-59ec-45b2-b394-6fc202070fda |
| 51042-692-41 | 2023-07-25 | C162847 | 48780-1 | 956f9ecf-d803-621f-e053-dbdaa90a74ad | 51260354-59ec-45b2-b394-6fc202070fda |
| 51042-692-17 | 2022-01-28 | C162847 | 48780-1 | 956f9ecf-d803-621f-e053-dbdaa90a74ad | 51260354-59ec-45b2-b394-6fc202070fda |
| 51042-692-41 | 2022-01-28 | C162847 | 48780-1 | 956f9ecf-d803-621f-e053-dbdaa90a74ad | 51260354-59ec-45b2-b394-6fc202070fda |
| 51042-692-17 | 2019-11-02 | C162847 | 48780-1 | 956f9ecf-d803-621f-e053-dbdaa90a74ad | 51260354-59ec-45b2-b394-6fc202070fda |
| 51042-692-41 | 2019-11-02 | C162847 | 48780-1 | 956f9ecf-d803-621f-e053-dbdaa90a74ad | 51260354-59ec-45b2-b394-6fc202070fda |
| 51042-692-17 | 2019-10-21 | C162847 | 48780-1 | 956f9ecf-d803-621f-e053-dbdaa90a74ad | 51260354-59ec-45b2-b394-6fc202070fda |
| 51042-692-41 | 2019-10-21 | C162847 | 48780-1 | 956f9ecf-d803-621f-e053-dbdaa90a74ad | 51260354-59ec-45b2-b394-6fc202070fda |