NDC properties for "Cetacaine 14 % / 2 % / 2 % Mucosal Spray" (RxCUI 1722107)
About this data
The tables show NDC propoerties for Cetacaine 14 % / 2 % / 2 % Mucosal Spray with the RxCUI 1722107
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 Cetacaine 14 % / 2 % / 2 % Mucosal Spray (RxCUI 1722107)
| MMSL_CODE | BD4037 |
|---|---|
| RxCUI | 1722107 |
| SPL_SET_ID | af1773c5-5d5b-4278-b551-30ad2df6d5b5 |
| Prescribable Synonym | Cetacaine 14 % / 2 % / 2 % Mucosal Spray |
| RXNAV_STR | Cetacaine 14 % / 2 % / 2 % Mucosal Spray |
| RxNorm Name | benzocaine 140 MG/ML / butamben 20 MG/ML / tetracaine 20 MG/ML Mucosal Spray [Cetacaine] |
| RxNorm Synonym | Cetacaine 14 % / 2 % / 2 % Mucosal Spray |
| Related queries | Interactions (for RxCUI 1722107) |
NDC Properties
NDC Item 00247054256
| NDC 10 | UNKNOWN |
|---|---|
| NDC Item | 00247054256 |
| Related queries | Properties for NDC 9 |
NDC Item 10223020101
| NDC 9 | 10223-0201 |
|---|---|
| NDC 10 | 10223-0201-1 |
| NDC Item | 10223020101 |
| Packaging | 1 BOTTLE, GLASS in 1 BOX (10223-0201-1) / 56 g in 1 BOTTLE, GLASS |
| FDA SPL set id | 614204 |
| Labeler | Cetylite Industries, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | UNAPPROVED DRUG OTHER |
| Marketing effective time low | 1958-01-01 |
| Marketing status | ACTIVE |
| UNAPPROVED_DRUG_OTHER | N/A |
| Related queries | Properties for NDC 9 10223-0201 |
NDC Item 10223020103
| NDC 9 | 10223-0201 |
|---|---|
| NDC 10 | 10223-0201-3 |
| NDC Item | 10223020103 |
| Packaging | 1 BOTTLE, GLASS in 1 BOX (10223-0201-3) / 20 g in 1 BOTTLE, GLASS |
| FDA SPL set id | 614204 |
| Labeler | Cetylite Industries, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | UNAPPROVED DRUG OTHER |
| Marketing effective time low | 1958-01-01 |
| Marketing status | ACTIVE |
| UNAPPROVED_DRUG_OTHER | N/A |
| Related queries | Properties for NDC 9 10223-0201 |
NDC Item 10223020104
| NDC 9 | 10223-0201 |
|---|---|
| NDC 10 | 10223-0201-4 |
| NDC Item | 10223020104 |
| Packaging | 1 BOTTLE, GLASS in 1 BOX (10223-0201-4) / 5 g in 1 BOTTLE, GLASS |
| FDA SPL set id | 614204 |
| Labeler | Cetylite Industries, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | UNAPPROVED DRUG OTHER |
| Marketing effective time low | 1958-01-01 |
| Marketing status | ACTIVE |
| UNAPPROVED_DRUG_OTHER | N/A |
| Related queries | Properties for NDC 9 10223-0201 |
NDC Item 00247054256
| NDC 10 | UNKNOWN |
|---|---|
| NDC Item | 00247054256 |
| Related queries | Properties for NDC 9 |
NDC Item 10223020101
| NDC 9 | 10223-0201 |
|---|---|
| NDC 10 | 10223-0201-1 |
| NDC Item | 10223020101 |
| Packaging | 1 BOTTLE, GLASS in 1 BOX (10223-0201-1) / 56 g in 1 BOTTLE, GLASS |
| FDA SPL set id | 614204 |
| Labeler | Cetylite Industries, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | UNAPPROVED DRUG OTHER |
| Marketing effective time low | 1958-01-01 |
| Marketing status | ACTIVE |
| UNAPPROVED_DRUG_OTHER | N/A |
| Related queries | Properties for NDC 9 10223-0201 |
NDC Item 10223020103
| NDC 9 | 10223-0201 |
|---|---|
| NDC 10 | 10223-0201-3 |
| NDC Item | 10223020103 |
| Packaging | 1 BOTTLE, GLASS in 1 BOX (10223-0201-3) / 20 g in 1 BOTTLE, GLASS |
| FDA SPL set id | 614204 |
| Labeler | Cetylite Industries, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | UNAPPROVED DRUG OTHER |
| Marketing effective time low | 1958-01-01 |
| Marketing status | ACTIVE |
| UNAPPROVED_DRUG_OTHER | N/A |
| Related queries | Properties for NDC 9 10223-0201 |
NDC Item 10223020104
| NDC 9 | 10223-0201 |
|---|---|
| NDC 10 | 10223-0201-4 |
| NDC Item | 10223020104 |
| Packaging | 1 BOTTLE, GLASS in 1 BOX (10223-0201-4) / 5 g in 1 BOTTLE, GLASS |
| FDA SPL set id | 614204 |
| Labeler | Cetylite Industries, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | UNAPPROVED DRUG OTHER |
| Marketing effective time low | 1958-01-01 |
| Marketing status | ACTIVE |
| UNAPPROVED_DRUG_OTHER | N/A |
| Related queries | Properties for NDC 9 10223-0201 |
NDC Item 00247054256
| NDC 10 | UNKNOWN |
|---|---|
| NDC Item | 00247054256 |
| Related queries | Properties for NDC 9 |
NDC Item 10223020101
| NDC 9 | 10223-0201 |
|---|---|
| NDC 10 | 10223-0201-1 |
| NDC Item | 10223020101 |
| Packaging | 1 BOTTLE, GLASS in 1 BOX (10223-0201-1) / 56 g in 1 BOTTLE, GLASS |
| FDA SPL set id | 614204 |
| Labeler | Cetylite Industries, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | UNAPPROVED DRUG OTHER |
| Marketing effective time low | 1958-01-01 |
| Marketing status | ACTIVE |
| UNAPPROVED_DRUG_OTHER | N/A |
| Related queries | Properties for NDC 9 10223-0201 |
NDC Item 10223020103
| NDC 9 | 10223-0201 |
|---|---|
| NDC 10 | 10223-0201-3 |
| NDC Item | 10223020103 |
| Packaging | 1 BOTTLE, GLASS in 1 BOX (10223-0201-3) / 20 g in 1 BOTTLE, GLASS |
| FDA SPL set id | 614204 |
| Labeler | Cetylite Industries, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | UNAPPROVED DRUG OTHER |
| Marketing effective time low | 1958-01-01 |
| Marketing status | ACTIVE |
| UNAPPROVED_DRUG_OTHER | N/A |
| Related queries | Properties for NDC 9 10223-0201 |
NDC Item 10223020104
| NDC 9 | 10223-0201 |
|---|---|
| NDC 10 | 10223-0201-4 |
| NDC Item | 10223020104 |
| Packaging | 1 BOTTLE, GLASS in 1 BOX (10223-0201-4) / 5 g in 1 BOTTLE, GLASS |
| FDA SPL set id | 614204 |
| Labeler | Cetylite Industries, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | UNAPPROVED DRUG OTHER |
| Marketing effective time low | 1958-01-01 |
| Marketing status | ACTIVE |
| UNAPPROVED_DRUG_OTHER | N/A |
| Related queries | Properties for NDC 9 10223-0201 |
NDC Item 00247054256
| NDC 10 | UNKNOWN |
|---|---|
| NDC Item | 00247054256 |
| Related queries | Properties for NDC 9 |
NDC Item 10223020101
| NDC 9 | 10223-0201 |
|---|---|
| NDC 10 | 10223-0201-1 |
| NDC Item | 10223020101 |
| Packaging | 1 BOTTLE, GLASS in 1 BOX (10223-0201-1) / 56 g in 1 BOTTLE, GLASS |
| FDA SPL set id | 614204 |
| Labeler | Cetylite Industries, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | UNAPPROVED DRUG OTHER |
| Marketing effective time low | 1958-01-01 |
| Marketing status | ACTIVE |
| UNAPPROVED_DRUG_OTHER | N/A |
| Related queries | Properties for NDC 9 10223-0201 |
NDC Item 10223020103
| NDC 9 | 10223-0201 |
|---|---|
| NDC 10 | 10223-0201-3 |
| NDC Item | 10223020103 |
| Packaging | 1 BOTTLE, GLASS in 1 BOX (10223-0201-3) / 20 g in 1 BOTTLE, GLASS |
| FDA SPL set id | 614204 |
| Labeler | Cetylite Industries, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | UNAPPROVED DRUG OTHER |
| Marketing effective time low | 1958-01-01 |
| Marketing status | ACTIVE |
| UNAPPROVED_DRUG_OTHER | N/A |
| Related queries | Properties for NDC 9 10223-0201 |
NDC Item 10223020104
| NDC 9 | 10223-0201 |
|---|---|
| NDC 10 | 10223-0201-4 |
| NDC Item | 10223020104 |
| Packaging | 1 BOTTLE, GLASS in 1 BOX (10223-0201-4) / 5 g in 1 BOTTLE, GLASS |
| FDA SPL set id | 614204 |
| Labeler | Cetylite Industries, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | UNAPPROVED DRUG OTHER |
| Marketing effective time low | 1958-01-01 |
| Marketing status | ACTIVE |
| UNAPPROVED_DRUG_OTHER | N/A |
| Related queries | Properties for NDC 9 10223-0201 |