NDC 68703-142 - DandRUUF Relief

This NDC is not currently matched to an FDA NDC product listing in FDA.report, but it is a valid NDC-form code. FDA.report is showing the available DailyMed label context for the product root.

Product NDC
68703-142
Package NDCs from labels
68703-142-59
Manufacturer
Native Remedies, LLC | King Bio
Effective date
2013-11-12
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
DandRUUF Relief - Native Remedies, LLC | King BioNative Remedies, LLC | King Bio2013-11-12OTC ANIMAL DRUG LABEL

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
68703-142DANDRUUF RELIEF (ALUMINA, APIS MELLIFICA, ARSENICUM IODATUM, CAUSTICUM, KALI MURIATICUM, SULPHUR) SPRAY [NATIVE REMEDIES, LLC]1Unmatched20131112_9c956689-9615-4ab6-8da7-bb63c0ba26d7.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
ALUMINUM OXIDEACTIVE INGREDIENTLMI26O6933DANDRUUF RELIEF (ALUMINA, APIS MELLIFICA, ARSENICUM IODATUM, CAUSTICUM, KALI MURIATICUM, SULPHUR) SPRAY [NATIVE REMEDIES, LLC]1
APIS MELLIFERAACTIVE INGREDIENT7S82P3R43ZDANDRUUF RELIEF (ALUMINA, APIS MELLIFICA, ARSENICUM IODATUM, CAUSTICUM, KALI MURIATICUM, SULPHUR) SPRAY [NATIVE REMEDIES, LLC]1
ARSENIC TRIIODIDEACTIVE INGREDIENT3029988O2TDANDRUUF RELIEF (ALUMINA, APIS MELLIFICA, ARSENICUM IODATUM, CAUSTICUM, KALI MURIATICUM, SULPHUR) SPRAY [NATIVE REMEDIES, LLC]1
CAUSTICUMACTIVE INGREDIENTDD5FO1WKFUDANDRUUF RELIEF (ALUMINA, APIS MELLIFICA, ARSENICUM IODATUM, CAUSTICUM, KALI MURIATICUM, SULPHUR) SPRAY [NATIVE REMEDIES, LLC]1
POTASSIUM CHLORIDEACTIVE INGREDIENT660YQ98I10DANDRUUF RELIEF (ALUMINA, APIS MELLIFICA, ARSENICUM IODATUM, CAUSTICUM, KALI MURIATICUM, SULPHUR) SPRAY [NATIVE REMEDIES, LLC]1
SULFURACTIVE INGREDIENT70FD1KFU70DANDRUUF RELIEF (ALUMINA, APIS MELLIFICA, ARSENICUM IODATUM, CAUSTICUM, KALI MURIATICUM, SULPHUR) SPRAY [NATIVE REMEDIES, LLC]1
ALUMINUM OXIDEACTIVE MOIETYLMI26O6933DANDRUUF RELIEF (ALUMINA, APIS MELLIFICA, ARSENICUM IODATUM, CAUSTICUM, KALI MURIATICUM, SULPHUR) SPRAY [NATIVE REMEDIES, LLC]1
APIS MELLIFERAACTIVE MOIETY7S82P3R43ZDANDRUUF RELIEF (ALUMINA, APIS MELLIFICA, ARSENICUM IODATUM, CAUSTICUM, KALI MURIATICUM, SULPHUR) SPRAY [NATIVE REMEDIES, LLC]1
ARSENIC CATION (3+)ACTIVE MOIETYC96613F5AVDANDRUUF RELIEF (ALUMINA, APIS MELLIFICA, ARSENICUM IODATUM, CAUSTICUM, KALI MURIATICUM, SULPHUR) SPRAY [NATIVE REMEDIES, LLC]1
CAUSTICUMACTIVE MOIETYDD5FO1WKFUDANDRUUF RELIEF (ALUMINA, APIS MELLIFICA, ARSENICUM IODATUM, CAUSTICUM, KALI MURIATICUM, SULPHUR) SPRAY [NATIVE REMEDIES, LLC]1
POTASSIUM CATIONACTIVE MOIETY295O53K152DANDRUUF RELIEF (ALUMINA, APIS MELLIFICA, ARSENICUM IODATUM, CAUSTICUM, KALI MURIATICUM, SULPHUR) SPRAY [NATIVE REMEDIES, LLC]1
SULFURACTIVE MOIETY70FD1KFU70DANDRUUF RELIEF (ALUMINA, APIS MELLIFICA, ARSENICUM IODATUM, CAUSTICUM, KALI MURIATICUM, SULPHUR) SPRAY [NATIVE REMEDIES, LLC]1
CITRIC ACID MONOHYDRATEINACTIVE INGREDIENT2968PHW8QPDANDRUUF RELIEF (ALUMINA, APIS MELLIFICA, ARSENICUM IODATUM, CAUSTICUM, KALI MURIATICUM, SULPHUR) SPRAY [NATIVE REMEDIES, LLC]1
POTASSIUM SORBATEINACTIVE INGREDIENT1VPU26JZZ4DANDRUUF RELIEF (ALUMINA, APIS MELLIFICA, ARSENICUM IODATUM, CAUSTICUM, KALI MURIATICUM, SULPHUR) SPRAY [NATIVE REMEDIES, LLC]1
WATERINACTIVE INGREDIENT059QF0KO0RDANDRUUF RELIEF (ALUMINA, APIS MELLIFICA, ARSENICUM IODATUM, CAUSTICUM, KALI MURIATICUM, SULPHUR) SPRAY [NATIVE REMEDIES, LLC]1

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 39 of 93 · 1,841 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
KLOR-CON MPOTASSIUM CHLORIDEUpsher-Smith Laboratories, LLCb89910f6-4ff5-4a62-8269-696f7c10e4f62025-07-14Warnings, Adverse reactionsExact identifier
unii: 660YQ98I10
Sterile WaterSTERILE WATERNephron Pharmaceuticals Corporationbc04a883-babc-87a6-e053-2995a90a3dfd2025-07-11Warnings, Adverse reactionsExact identifier
unii: 059QF0KO0R
POTASSIUM CHLORIDE IN SODIUM CHLORIDESODIUM CHLORIDE AND POTASSIUM CHLORIDEB. Braun Medical Inc.ecc38772-246a-46c4-b42a-b9b81124f27f2025-07-11Warnings, Adverse reactionsExact identifier
unii: 660YQ98I10
Potassium ChloridePOTASSIUM CHLORIDEUpsher-SmithLaboratories, LLCad584ce4-a64d-4851-80e9-0eeedc0b9d062025-07-10Warnings, Adverse reactionsExact identifier
unii: 660YQ98I10
PlexionSULFACETAMIDE SODIUM, SULFURCintex Services, LLC399a01bb-e454-3e20-e063-6294a90ab17c2025-07-10Warnings, Adverse reactionsExact identifier
unii: 70FD1KFU70
SODIUM SULFACETAMIDE, SULFURSULFACETAMIDE SODIUM AND SULFURWestminster Pharmaceuticals, LLC6b7e2859-d149-4116-bd98-d6d096266b042025-07-01Warnings, Adverse reactionsExact identifier
unii: 70FD1KFU70
Schuessler Tissue Salts Kali Mur Glandular Tonic 5KALI MURIATICUMMartin & Pleasance Pty Ltd4b2d8d03-c829-4292-ad94-993376d81b8f2025-07-01WarningsExact identifier
unii: 660YQ98I10
BacAPIS MELLIFERA, ARSENIC TRIOXIDE, ATROPA BELLADONNA, MATRICARIA CHAMOMILLA FLOWERING TOP OIL, LACHESIS MUTA VENOM, MERCURIUS SOLUBILIS, PULSATILLA VULGARIS WHOLE, TOXICODENDRON PUBESCENS LEAF, AND SILICON DIOXIDEZorex7ae38e0c-8e74-4fd5-8605-45e424a84d012025-06-30WarningsExact identifier
unii: 7S82P3R43Z
Betula ArgentumBETULA ARGENTUMUriel Pharmacy Inc.7f436fc5-0983-4ce3-9951-e68e395bcab02025-06-27WarningsExact identifier
unii: 7S82P3R43Z
Potassium ChloridePOTASSIUM CHLORIDEAmerican Health Packagingb165ad93-1dc1-4863-9f0b-d7b97c42c94c2025-06-23Warnings, Adverse reactionsExact identifier
unii: 660YQ98I10
Plaque identifyingPLAQUE IDENTIFYINGShenzhen Yagao Technology Co., Ltd.37eeb656-22f1-7372-e063-6394a90ad0412025-06-19WarningsExact identifier
unii: 059QF0KO0R
Potassium Chloride ERPOTASSIUM CHLORIDE ERDirect_Rx377854ff-8034-c7ac-e063-6294a90a08172025-06-13Warnings, Adverse reactionsExact identifier
unii: 660YQ98I10
Margarite Zinc CreamZINC CREAMRenu Laboratories, LLC3ca3b7d8-702a-036b-e054-00144ff8d46c2025-06-10WarningsExact identifier
unii: 70FD1KFU70
HAIR STIMPEDICULUS CAPITIS, THYROIDINUM (SUIS), BARYTA CARBONICA, BORAX, CALCAREA CARBONICA, CINCHONA OFFICINALIS, GLANDULA SUPRARENALIS SUIS, HYDROFLUORICUM ACIDUM, MERCURIUS SOLUBILIS, MEZEREUM, NATRUM MURIATICUM, PHOSPHORUS, PULSATILLA (PRATENSIS), SEPIA, SILICEA, SULPHUR, THUJA OCCIDENTALIS, VINCA MINORThe Wellness Center for Research and Education, Inc.8ecc05ff-ed5a-4157-9100-1c7912686f072025-06-06WarningsExact identifier
unii: 70FD1KFU70
MBM 13 FemalePHYTOLACCA DECANDRA, HYPOPHYSIS (SUIS), SCROPHULARIA NODOSA, HYPOTHALAMUS (SUIS), CALCAREA CARBONICA, CIMICIFUGA RACEMOSA, LILIUM TIGRINUM, SULPHUR, CAUSTICUM, GRAPHITES, KALI PHOSPHORICUMThe Wellness Center for Research and Education, Inc.2ba45d16-58d8-4921-ae06-0cec43238dd32025-06-06WarningsExact identifier
unii: DD5FO1WKFU
unii: 70FD1KFU70
SODIUM SULFACETAMIDE AND SULFURSULFACETAMIDE SODIUM, SULFURBioComp Pharma, Inc.1ba8e7a0-d700-c96b-e063-6394a90a04632025-06-05Warnings, Adverse reactionsExact identifier
unii: 70FD1KFU70
SODIUM SULFACETAMIDE AND SULFURSODIUM SULFACETAMIDE 9.8% AND SULFUR 4.8%BioComp Pharma, Inc.1ba8bb47-6f7a-28ec-e063-6394a90a8eb32025-06-05Warnings, Adverse reactionsExact identifier
unii: 70FD1KFU70
MBM 7 LungCOCCUS CACTI, LUNG (SUIS), IGNATIA AMARA, CAUSTICUM, NATRUM MURIATICUMThe Wellness Center for Research and Education, Inc.6eb49fb5-485c-4b48-b231-4db88ebe20df2025-06-04WarningsExact identifier
unii: DD5FO1WKFU
SULFACETAMIDE SODIUM, SULFURSULFACETAMIDE SODIUM, SULFURBantry Pharma, LLCf433db67-d8a6-320e-e053-2995a90aab522025-06-04Warnings, Adverse reactionsExact identifier
unii: 70FD1KFU70
PRISMASOL BGK2/0MAGNESIUM CHLORIDE, DEXTROSE ANHYDROUS, LACTIC ACID, SODIUM CHLORIDE, SODIUM BICARBONATE, AND POTASSIUM CHLORIDEVantive US Healthcare LLC7f675fee-8940-4ece-bb0c-75ac79d8708c2025-05-31Warnings, Adverse reactionsExact identifier
unii: 660YQ98I10

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.