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 |