Document Type including Content of Labeling Type
Source: Logical Observation Identifiers Names and Codes
LOINC OID: 2.16.840.1.113883.6.1
|
LOINC Code |
LOINC Name |
|---|---|
| 98075-5 | ANIMAL CELLS, TISSUES, AND CELL AND TISSUE BASED PRODUCT LABEL |
| 77647-6 | ANIMAL COMPOUNDED DRUG LABEL |
| 104091-4 | ANIMAL DRUG FOR FURTHER PROCESSING |
| 86445-4 | BLANKET NO CHANGES CERTIFICATION OF PRODUCT LISTING |
| 53409-9 | BULK INGREDIENT |
| 81203-2 | BULK INGREDIENT - ANIMAL DRUG |
| 60684-8 | CELLULAR THERAPY |
| 58474-8 | COSMETIC |
| 103573-2 | COSMETIC FACILITY REGISTRATION |
| 104087-2 | COSMETIC FACILITY REGISTRATION-ABBREVIATED RENEWAL |
| 104086-4 | COSMETIC FACILITY REGISTRATION-AMENDMENT |
| 104089-8 | COSMETIC FACILITY REGISTRATION-BIENNIAL RENEWAL |
| 104088-0 | COSMETIC FACILITY REGISTRATION-CANCELLATION |
| 103572-4 | COSMETIC PRODUCT LISTING |
| 105122-6 | COSMETIC UPDATE |
| 104090-6 | COSMETIC-ABBREVIATED RENEWAL |
| 58476-3 | DIETARY SUPPLEMENT |
| 78744-0 | DRUG FOR FURTHER PROCESSING |
| 70097-1 | ESTABLISHMENT DE-REGISTRATION |
| 51725-0 | ESTABLISHMENT REGISTRATION |
| 89600-1 | FDA-INITIATED COMPLIANCE ACTION DRUG REGISTRATION AND DRUG LISTING INACTIVATION |
| 99282-6 | FDA-INITIATED COMPLIANCE ACTION DRUG REGISTRATION AND DRUG LISTING INACTIVATION - ANIMAL DRUG |
| 71743-9 | GENERIC DRUG FACILITY IDENTIFICATION SUBMISSION |
| 75031-5 | HUMAN COMPOUNDED DRUG LABEL |
| 34390-5 | HUMAN OTC DRUG LABEL |
| 34391-3 | HUMAN PRESCRIPTION DRUG LABEL |
| 72090-4 | IDENTIFICATION OF CBER-REGULATED GENERIC DRUG FACILITY |
| 71446-9 | INDEXING - BILLING UNIT |
| 77648-4 | INDEXING - BIOLOGICAL DRUG SUBSTANCE |
| 93723-5 | INDEXING - DRUG INTERACTIONS |
| 63417-0 | INDEXING - INDICATION |
| 93372-1 | INDEXING - NATIONAL CLINICAL TRIALS NUMBER |
| 60685-5 | INDEXING - PHARMACOLOGIC CLASS |
| 73815-3 | INDEXING - PRODUCT CONCEPT |
| 82353-4 | INDEXING - RISK EVALUATION & MITIGATION STRATEGIES |
| 64124-1 | INDEXING - SUBSTANCE |
| 77288-9 | INDEXING - WARNING LETTER ALERT |
| 101437-2 | INTENTIONAL ANIMAL GENOMIC ALTERATION LABEL |
| 53407-3 | LICENSE BLOOD INTERMEDIATES/PASTE LABEL |
| 53408-1 | LICENSED MINIMALLY MANIPULATED CELLS LABEL |
| 53406-5 | LICENSED VACCINE BULK INTERMEDIATE LABEL |
| 66105-8 | LOT DISTRIBUTION DATA |
| 55439-4 | MEDICAL DEVICE |
| 58475-5 | MEDICAL FOOD |
| 53410-7 | NO CHANGE NOTIFICATION |
| 53405-7 | NON-STANDARDIZED ALLERGENIC LABEL |
| 69968-6 | NDC LABELER CODE INACTIVATION |
| 81204-0 | NDC LABELER CODE INACTIVATION - ANIMAL DRUG |
| 72871-7 | NDC LABELER CODE REQUEST - ANIMAL DRUG |
| 51726-8 | NDC/NHRIC LABELER CODE REQUEST |
| 50577-6 | OTC ANIMAL DRUG LABEL |
| 69403-4 | OTC MEDICAL DEVICE LABEL |
| 50576-8 | OTC TYPE A MEDICATED ARTICLE ANIMAL DRUG LABEL |
| 50574-3 | OTC TYPE B MEDICATED FEED ANIMAL DRUG LABEL |
| 50573-5 | OTC TYPE C MEDICATED FEED ANIMAL DRUG LABEL |
| 53411-5 | OUT OF BUSINESS NOTIFICATION |
| 60683-0 | PLASMA DERIVATIVE |
| 50578-4 | PRESCRIPTION ANIMAL DRUG LABEL |
| 69404-2 | PRESCRIPTION MEDICAL DEVICE LABEL |
| 78745-7 | RECOMBINANT DEOXYRIBONUCLEIC ACID CONSTRUCT LABEL |
| 85274-9 | REMS RELEASE |
| 82351-8 | RISK EVALUATION & MITIGATION STRATEGIES |
| 60682-2 | STANDARDIZED ALLERGENIC |
| 53404-0 | VACCINE LABEL |
| 50575-0 | VFD TYPE A MEDICATED ARTICLE ANIMAL DRUG LABEL |
| 50572-7 | VFD TYPE B MEDICATED FEED ANIMAL DRUG LABEL |
| 50571-9 | VFD TYPE C MEDICATED FEED ANIMAL DRUG LABEL |
| 75030-7 | WHOLESALE DRUG DISTRIBUTORS AND THIRD-PARTY LOGISTICS FACILITY REPORT |
| 77573-4 | WITHDRAWAL OF WHOLESALE DRUG DISTRIBUTORS AND THIRD-PARTY LOGISTICS FACILITY REPORT |