NDC properties for "tetracaine 1 % Topical Cream" (RxCUI 313246)
About this data
The tables show NDC propoerties for tetracaine 1 % Topical Cream with the RxCUI 313246
This product uses publicly available data from the U.S. National Library of Medicine (NLM), National Institutes of Health, Department of Health and Human Services; NLM is not responsible for the product and does not endorse or recommend this or any other product
Details for tetracaine 1 % Topical Cream (RxCUI 313246)
| MMSL_CODE | CD4846 |
|---|---|
| RxCUI | 313246 |
| SNOMEDCT | 331628004 |
| SPL_SET_ID | 3a477714-6ff3-62aa-e054-00144ff8d46c |
| SPL_SET_ID | 3a5cf648-cc76-620e-e054-00144ff8d46c |
| SPL_SET_ID | b95bad36-668d-0954-e053-2995a90ab0f3 |
| VUID | 4004339 |
| Prescribable Synonym | tetracaine HCl 1 % Topical Cream |
| RXNAV_STR | tetracaine 10 MG/ML Topical Cream |
| RxNorm Name | tetracaine 10 MG/ML Topical Cream |
| RxNorm Synonym | tetracaine 1 % Topical Cream |
| Related queries | Interactions (for RxCUI 313246) |
NDC Properties
NDC Item 37945021234
| NDC 9 | 37945-212 |
|---|---|
| NDC 10 | 37945-212-34 |
| NDC Item | 37945021234 |
| Packaging | 10 mL in 1 TUBE |
| FDA SPL set id | 435801 |
| Labeler | Bio-Medical & Pharmaceutical Manufacturing Corporation |
| Label type | HUMAN OTC DRUG |
| Marketing category | OTC MONOGRAPH NOT FINAL |
| Marketing effective time low | 2016-08-19 |
| Marketing status | ACTIVE |
| OTC monograph not final | part348 |
| Related queries | Properties for NDC 9 37945-212 |
NDC Item 70704021234
| NDC 9 | 70704-212 |
|---|---|
| NDC 10 | 70704-212-34 |
| NDC Item | 70704021234 |
| Packaging | 10 mL in 1 TUBE |
| FDA SPL set id | 350348 |
| FDA SPL set id | 561388 |
| Labeler | Burn Solution Foundations |
| Label type | HUMAN OTC DRUG |
| Marketing category | OTC MONOGRAPH NOT FINAL |
| Marketing effective time low | 2016-08-23 |
| Marketing effective time low | 2021-02-02 |
| Marketing status | ACTIVE |
| OTC monograph not final | part348 |
| Related queries | Properties for NDC 9 70704-212 |
NDC Item 37945021234
| NDC 9 | 37945-212 |
|---|---|
| NDC 10 | 37945-212-34 |
| NDC Item | 37945021234 |
| Packaging | 10 mL in 1 TUBE |
| FDA SPL set id | 435801 |
| Labeler | Bio-Medical & Pharmaceutical Manufacturing Corporation |
| Label type | HUMAN OTC DRUG |
| Marketing category | OTC MONOGRAPH NOT FINAL |
| Marketing effective time low | 2016-08-19 |
| Marketing status | ACTIVE |
| OTC monograph not final | part348 |
| Related queries | Properties for NDC 9 37945-212 |
NDC Item 70704021234
| NDC 9 | 70704-212 |
|---|---|
| NDC 10 | 70704-212-34 |
| NDC Item | 70704021234 |
| Packaging | 10 mL in 1 TUBE |
| FDA SPL set id | 350348 |
| FDA SPL set id | 561388 |
| Labeler | Burn Solution Foundations |
| Label type | HUMAN OTC DRUG |
| Marketing category | OTC MONOGRAPH NOT FINAL |
| Marketing effective time low | 2016-08-23 |
| Marketing effective time low | 2021-02-02 |
| Marketing status | ACTIVE |
| OTC monograph not final | part348 |
| Related queries | Properties for NDC 9 70704-212 |