NDC properties for "Viabecline 0.03 MG/MG Topical Ointment" (RxCUI 1926470)
About this data
The tables show NDC propoerties for Viabecline 0.03 MG/MG Topical Ointment with the RxCUI 1926470
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 Viabecline 0.03 MG/MG Topical Ointment (RxCUI 1926470)
| RxCUI | 1926470 |
|---|---|
| SPL_SET_ID | 9fd7041a-6c23-4332-90fe-759bb4aea2ae |
| Prescribable Synonym | VIABECLINE 3 % Topical Ointment |
| RXNAV_STR | Viabecline 3 % Topical Ointment |
| RxNorm Name | tetracycline hydrochloride 0.03 MG/MG Topical Ointment [Viabecline] |
| RxNorm Synonym | Viabecline 0.03 MG/MG Topical Ointment |
| RxNorm Synonym | Viabecline 3 % Topical Ointment |
| Related queries | Interactions (for RxCUI 1926470) |
NDC Properties
NDC Item 71491010000
| NDC 9 | 71491-100 |
|---|---|
| NDC 10 | 71491-100-00 |
| NDC Item | 71491010000 |
| Packaging | 5 mL in 1 BOTTLE, DROPPER (71491-100-00) |
| FDA SPL set id | 750568 |
| Labeler | Accuria, LLC |
| Label type | HUMAN OTC DRUG |
| Marketing category | OTC MONOGRAPH DRUG |
| Marketing effective time low | 2017-06-14 |
| Marketing status | ACTIVE |
| OTC_MONOGRAPH_DRUG | M004 |
| Related queries | Properties for NDC 9 71491-100 |
NDC Item 71491010001
| NDC 9 | 71491-100 |
|---|---|
| NDC 10 | 71491-100-01 |
| NDC Item | 71491010001 |
| Packaging | 15 mL in 1 BOTTLE, DROPPER (71491-100-01) |
| FDA SPL set id | 750568 |
| Labeler | Accuria, LLC |
| Label type | HUMAN OTC DRUG |
| Marketing category | OTC MONOGRAPH DRUG |
| Marketing effective time low | 2017-06-14 |
| Marketing status | ACTIVE |
| OTC_MONOGRAPH_DRUG | M004 |
| Related queries | Properties for NDC 9 71491-100 |
NDC Item 71491010000
| NDC 9 | 71491-100 |
|---|---|
| NDC 10 | 71491-100-00 |
| NDC Item | 71491010000 |
| Packaging | 5 mL in 1 BOTTLE, DROPPER (71491-100-00) |
| FDA SPL set id | 750568 |
| Labeler | Accuria, LLC |
| Label type | HUMAN OTC DRUG |
| Marketing category | OTC MONOGRAPH DRUG |
| Marketing effective time low | 2017-06-14 |
| Marketing status | ACTIVE |
| OTC_MONOGRAPH_DRUG | M004 |
| Related queries | Properties for NDC 9 71491-100 |
NDC Item 71491010001
| NDC 9 | 71491-100 |
|---|---|
| NDC 10 | 71491-100-01 |
| NDC Item | 71491010001 |
| Packaging | 15 mL in 1 BOTTLE, DROPPER (71491-100-01) |
| FDA SPL set id | 750568 |
| Labeler | Accuria, LLC |
| Label type | HUMAN OTC DRUG |
| Marketing category | OTC MONOGRAPH DRUG |
| Marketing effective time low | 2017-06-14 |
| Marketing status | ACTIVE |
| OTC_MONOGRAPH_DRUG | M004 |
| Related queries | Properties for NDC 9 71491-100 |