NDC properties for "tetracycline hydrochloride 30 MG/ML Topical Spray" (RxCUI 2180656)
About this data
The tables show NDC propoerties for tetracycline hydrochloride 30 MG/ML Topical Spray with the RxCUI 2180656
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 tetracycline hydrochloride 30 MG/ML Topical Spray (RxCUI 2180656)
| RxCUI | 2180656 |
|---|---|
| SPL_SET_ID | 0961b097-ba41-40c2-aaec-dd291841bf09 |
| SPL_SET_ID | 93a6e02e-9f4b-4821-afa2-2029769f3088 |
| SPL_SET_ID | f2bc68ac-5563-4ade-a75d-6517a7e97f72 |
| Prescribable Synonym | tetracycline HCl 3 % Topical Spray |
| RXNAV_STR | tetracycline hydrochloride 30 MG/ML Topical Spray |
| RxNorm Name | tetracycline hydrochloride 30 MG/ML Topical Spray |
| Related queries | Interactions (for RxCUI 2180656) |
NDC Properties
NDC Item 71262001001
| NDC 9 | 71262-010 |
|---|---|
| NDC 10 | 71262-010-01 |
| NDC Item | 71262001001 |
| Packaging | 1 BOTTLE in 1 CARTON (71262-010-01) / 55 mL in 1 BOTTLE |
| FDA SPL set id | 857139 |
| Labeler | VIADERMA DISTRIBUTION INC |
| Label type | HUMAN OTC DRUG |
| Marketing category | OTC MONOGRAPH DRUG |
| Marketing effective time low | 2024-05-01 |
| Marketing status | ACTIVE |
| OTC_MONOGRAPH_DRUG | M004 |
| Related queries | Properties for NDC 9 71262-010 |
NDC Item 85494000001
| NDC 9 | 85494-000 |
|---|---|
| NDC 10 | 85494-000-01 |
| NDC Item | 85494000001 |
| Packaging | 1 BOTTLE, SPRAY in 1 BOX (85494-000-01) / 50 mL in 1 BOTTLE, SPRAY |
| FDA SPL set id | 869193 |
| Labeler | HONESTLY LLC |
| Label type | HUMAN OTC DRUG |
| Marketing category | OTC MONOGRAPH DRUG |
| Marketing effective time low | 2025-03-03 |
| Marketing status | active |
| OTC_MONOGRAPH_DRUG | M004 |
| Related queries | Properties for NDC 9 85494-000 |
NDC Item 71262001001
| NDC 9 | 71262-010 |
|---|---|
| NDC 10 | 71262-010-01 |
| NDC Item | 71262001001 |
| Packaging | 1 BOTTLE in 1 CARTON (71262-010-01) / 55 mL in 1 BOTTLE |
| FDA SPL set id | 857139 |
| Labeler | VIADERMA DISTRIBUTION INC |
| Label type | HUMAN OTC DRUG |
| Marketing category | OTC MONOGRAPH DRUG |
| Marketing effective time low | 2024-05-01 |
| Marketing status | ACTIVE |
| OTC_MONOGRAPH_DRUG | M004 |
| Related queries | Properties for NDC 9 71262-010 |
NDC Item 85494000001
| NDC 9 | 85494-000 |
|---|---|
| NDC 10 | 85494-000-01 |
| NDC Item | 85494000001 |
| Packaging | 1 BOTTLE, SPRAY in 1 BOX (85494-000-01) / 50 mL in 1 BOTTLE, SPRAY |
| FDA SPL set id | 869193 |
| Labeler | HONESTLY LLC |
| Label type | HUMAN OTC DRUG |
| Marketing category | OTC MONOGRAPH DRUG |
| Marketing effective time low | 2025-03-03 |
| Marketing status | active |
| OTC_MONOGRAPH_DRUG | M004 |
| Related queries | Properties for NDC 9 85494-000 |