FD&C BLUE NO. 2

Substance profile for UNII L06K8R7DQK, enriched with FDA NDC listings, DailyMed labels, legacy aliases, and open chemistry identifiers.

Chemical structure for FD&C BLUE NO. 2
Structure render from NCI/CADD chemical resolver

Substance Identity#

UNII
L06K8R7DQK
Preferred term
FD&C BLUE NO. 2
Registry number
860-22-0
Ingredient type
INGREDIENT SUBSTANCE
Chemical structure for FD&C BLUE NO. 2
Structure render from NCI/CADD chemical resolver

Chemical And Database Identifiers#

RxCUI
0
PubChem
0
NCIt
C71675
INN ID
0

Open Chemistry Sources#

Source, Identifier, Link table
SourceIdentifierLink
NCI ThesaurusC71675https://ncit.nci.nih.gov/ncitbrowser/ConceptReport.jsp?dictionary=NCI_Thesaurus&code=C71675
FDA Substance Registration SystemL06K8R7DQKhttps://precision.fda.gov/uniisearch/srs/unii/L06K8R7DQK

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
FD&C BLUE NO. 2INACTIVE INGREDIENTL06K8R7DQKGLIMEPIRIDE1
FD&C BLUE NO. 2INACTIVE INGREDIENTL06K8R7DQKNAPROXEN Tablets, USP NAPROXEN SODIUM Tablets, USP1
FD&C BLUE NO. 2INACTIVE INGREDIENTL06K8R7DQKESZOPICLONE1
FD&C BLUE NO. 2INACTIVE INGREDIENTL06K8R7DQKAZITHROMYCIN1
FD&C BLUE NO. 2INACTIVE INGREDIENTL06K8R7DQKETODOLAC3
FD&C BLUE NO. 2INACTIVE INGREDIENTL06K8R7DQKZOLPIDEM TARTRATE4
FD&C BLUE NO. 2INACTIVE INGREDIENTL06K8R7DQKDOCUSATE SODIUM AND SENNA2
FD&C BLUE NO. 2INACTIVE INGREDIENTL06K8R7DQKLEVETIRACETAM3
FD&C BLUE NO. 2INACTIVE INGREDIENTL06K8R7DQKGLIMEPIRIDE1
FD&C BLUE NO. 2INACTIVE INGREDIENTL06K8R7DQKLISINOPRIL AND HYDROCHLOROTHIAZIDE1
FD&C BLUE NO. 2INACTIVE INGREDIENTL06K8R7DQKZONISAMIDE1
FD&C BLUE NO. 2INACTIVE INGREDIENTL06K8R7DQK14db4981-5e50-4551-84f0-24f2c833d6291
FD&C BLUE NO. 2INACTIVE INGREDIENTL06K8R7DQKALPRAZOLAM1
FD&C BLUE NO. 2INACTIVE INGREDIENTL06K8R7DQKDrug Facts2
FD&C BLUE NO. 2INACTIVE INGREDIENTL06K8R7DQKThese highlights do not include all the information needed to use Gabapentin capsules safely and effectively. See full prescribing information for gabapentin capsules. Gabapentin Capsules, USP for oral use Initial U.S. Approval: 19931
FD&C BLUE NO. 2INACTIVE INGREDIENTL06K8R7DQKL-METHYLFOLATE CALCIUM 7.5mg Tablets L-METHYLFOLATE CALCIUM 15mg Tablets4
FD&C BLUE NO. 2INACTIVE INGREDIENTL06K8R7DQKMORPHINE SULFATE2
FD&C BLUE NO. 2INACTIVE INGREDIENTL06K8R7DQKZonisamide1
FD&C BLUE NO. 2INACTIVE INGREDIENTL06K8R7DQKThese highlights do not include all the information needed to use valacyclovir tablets, USP safely and effectively. See full prescribing information for valacyclovir tablets, USP. VALACYCLOVIR TABLETS USP Initial U.S. Approval: 19951
FD&C BLUE NO. 2INACTIVE INGREDIENTL06K8R7DQKDIVALPROEX SODIUM2
FD&C BLUE NO. 2INACTIVE INGREDIENTL06K8R7DQKESZOPICLONE2
FD&C BLUE NO. 2INACTIVE INGREDIENTL06K8R7DQKdoxepin hydrochloride2
FD&C BLUE NO. 2INACTIVE INGREDIENTL06K8R7DQKAlprazolam Tablets, USP2
FD&C BLUE NO. 2INACTIVE INGREDIENTL06K8R7DQKLAMOTRIGINE1
FD&C Blue No. 2INACTIVE INGREDIENTL06K8R7DQKMetolazone Tablets, USP3
FD&C BLUE NO. 2INACTIVE INGREDIENTL06K8R7DQKThese highlights do not include all the information needed to use memantine hydrochloride safely and effectively. See full prescribing information for memantine hydrochloride. MEMANTINE hydrochloride tablets, for oral use Initial U.S. Approval: 20031
FD&C BLUE NO. 2INACTIVE INGREDIENTL06K8R7DQKThese highlights do not include all the information needed to use Dextroamphetamine Saccharate, Amphetamine Aspartate Monohydrate, Dextroamphetamine Sulfate and Amphetamine Sulfate Extended-Release Capsules (MAS-ER) safely and effectively. See full prescribing information for MAS-ER Capsules. Dextroamphetamine Saccharate, Amphetamine Aspartate Monohydrate, Dextroamphetamine Sulfate and Amphetamine Sulfate Extended-Release Capsules (mixed salts of a single-entity amphetamine product), CII Initial U.S. Approv17
FD&C BLUE NO. 2INACTIVE INGREDIENTL06K8R7DQKThese highlights do not include all the information needed to use VIAGRA safely and effectively. See full prescribing information for VIAGRA. VIAGRA® (sildenafil citrate) tablets, for oral use Initial U.S. Approval: 19984
FD&C BLUE NO. 2INACTIVE INGREDIENTL06K8R7DQKThese highlights do not include all the information needed to use phentermine hydrochloride capsules, USP safely and effectively. See full prescribing information for phentermine hydrochloride capsules, USP. PHENTERMINE Hydrochloride Capsules, USP CIV Initial U.S. Approval: 19592
FD&C BLUE NO. 2INACTIVE INGREDIENTL06K8R7DQK344f908c-934e-4c98-aeef-68fd09d47c721
FD&C BLUE NO. 2INACTIVE INGREDIENTL06K8R7DQKSomnapure Clinical Strength1
FD&C BLUE NO. 2INACTIVE INGREDIENTL06K8R7DQKLevothyroxine Sodium Tablets, USP4
FD&C BLUE NO. 2INACTIVE INGREDIENTL06K8R7DQKLevothyroxine Sodium Tablets, USP1
FD&C BLUE NO. 2INACTIVE INGREDIENTL06K8R7DQKThese highlights do not include all the information needed to use oxybutynin chloride extended-release tablets safely and effectively. See full prescribing information for oxybutynin chloride extended-release tablets. Oxybutynin Chloride Extended-Release Tablets for oral use Initial U.S. Approval: 19751001
FD&C BLUE NO. 2INACTIVE INGREDIENTL06K8R7DQKTriamterene and Hydrochlorothiazide Tablets USP Revised: April 2012 Rx only1
FD&C BLUE NO. 2INACTIVE INGREDIENTL06K8R7DQKThese highlights do not include all the information needed to use zolpidem tartrate tablets, USP safely and effectively. See full prescribing information for zolpidem tartrate tablets, USP ZOLPIDEM Tartrate Tablets, USP, for oral use CIV Initial U.S. Approval: 19921
FD&C BLUE NO. 2INACTIVE INGREDIENTL06K8R7DQKHydrochlorothiazide Capsules, USP Revised: October 2011 Rx only 174788-31
FD&C BLUE NO. 2INACTIVE INGREDIENTL06K8R7DQKHydrochlorothiazide Capsules, USP Revised: October 2011 Rx only 174788-31
FD&C BLUE NO. 2INACTIVE INGREDIENTL06K8R7DQKNaproxen Sodium Tablets, USP 275 mg and 550 mg1
FD&C BLUE NO. 2INACTIVE INGREDIENTL06K8R7DQKUrsodiol Capsules, USP2
FD&C BLUE NO. 2INACTIVE INGREDIENTL06K8R7DQKDOXYCYCLINE HYCLATE TABLETS, USP Rev. 11/14 Rx Only1
FD&C BLUE NO. 2INACTIVE INGREDIENTL06K8R7DQKNiva-Plus™ Tablets1
FD&C BLUE NO. 2INACTIVE INGREDIENTL06K8R7DQKPilocarpine Hydrochloride Tablets, USP1
FD&C BLUE NO. 2INACTIVE INGREDIENTL06K8R7DQKPROCHLORPERAZINE MALEATE TABLETS USP Rx Only1
FD&C BLUE NO. 2INACTIVE INGREDIENTL06K8R7DQKTamsulosin hydrochloride capsules USP, 0.4 mg These highlights do not include all the information needed to use Tamsulosin hydrochloride safely and effectively. See full prescribing information for Tamsulosin hydrochloride. Tamsulosin hydrochloride (Tamsulosin hydrochloride) CAPSULE for ORAL use. Initial U.S. Approval: 19971
FD&C BLUE NO. 2INACTIVE INGREDIENTL06K8R7DQKDOXYCYCLINE HYCLATE CAPSULES, USP2
FD&C BLUE NO. 2INACTIVE INGREDIENTL06K8R7DQKThese highlights do not include all the information needed to use RISPERIDONE safely and effectively. See full prescribing information for RISPERIDONE. RISPERIDONE TABLETS USP, for oral use Initial U.S. Approval: 19931
FD&C BLUE NO. 2INACTIVE INGREDIENTL06K8R7DQKThese highlights do not include all the information needed to use levetiracetam tablets safely and effectively. See full prescribing information for levetiracetam tablets USP. Levetiracetam Tablets USP for Oral Use Initial U.S. Approval: 19992
FD&C BLUE NO. 2INACTIVE INGREDIENTL06K8R7DQKThese highlights do not include all the information needed to use clopidogrel tablets USP safely and effectively. See full prescribing information for clopidogrel tablets USP. CLOPIDOGREL tablets USP for oral use Initial U.S. Approval: 19971
FD&C BLUE NO. 2INACTIVE INGREDIENTL06K8R7DQKDrug Facts1
FD&C BLUE NO. 2INACTIVE INGREDIENTL06K8R7DQKCold-EEZE ® Daytime/Nighttime QuickMelts ®1
FD&C BLUE NO. 2INACTIVE INGREDIENTL06K8R7DQKNaproxen Sodium Tablets, USP 275 mg and 550 mg2
FD&C BLUE NO. 2INACTIVE INGREDIENTL06K8R7DQKCyclobenzaprine Hydrochloride Tablets, USP1
FD&C BLUE NO. 2INACTIVE INGREDIENTL06K8R7DQKALPRAZOLAM TABLETS, USP CIV2
FD&C Blue No. 2INACTIVE INGREDIENTL06K8R7DQKChildren's Pain Relief1
FD&C BLUE NO. 2INACTIVE INGREDIENTL06K8R7DQK392476e1-49fd-4014-bb52-b31937077c333
FD&C BLUE NO. 2INACTIVE INGREDIENTL06K8R7DQKb4189b86-b109-4828-9bcb-38e9dbc248db1
FD&C BLUE NO. 2INACTIVE INGREDIENTL06K8R7DQKRx only2
FD&C BLUE NO. 2INACTIVE INGREDIENTL06K8R7DQKSELECT-OB ® Prenatal Supplement1
FD&C BLUE NO. 2INACTIVE INGREDIENTL06K8R7DQKAMITRIPTYLINE HYDROCHLORIDE TABLETS, USP4
FD&C BLUE NO. 2INACTIVE INGREDIENTL06K8R7DQKFalessa Kit5
FD&C BLUE NO. 2INACTIVE INGREDIENTL06K8R7DQKIsotretinoin Capsules USP1
FD&C BLUE NO. 2INACTIVE INGREDIENTL06K8R7DQKHYDROXYZINE PAMOATE CAPSULES USP4
FD&C BLUE NO. 2INACTIVE INGREDIENTL06K8R7DQKdalan Therapy liquid antibacterial hand soap ANTIBACTERIAL & odor neutralizer1
FD&C BLUE NO. 2INACTIVE INGREDIENTL06K8R7DQKSELECT-OB ® Chewable Caplets Prenatal Supplement1
FD&C BLUE NO. 2INACTIVE INGREDIENTL06K8R7DQKUnknown Title1000
FD&C BLUE NO. 2INACTIVE INGREDIENTL06K8R7DQKThese highlights do not include all the information needed to use divalproex sodium extended-release tablets USP safely and effectively. See full prescribing information for divalproex sodium extended-release tablets USP. DIVALPROEX Sodium Extended-Release Tablets USP, for Oral Use Initial U.S. Approval: 20002
FD&C BLUE NO. 2INACTIVE INGREDIENTL06K8R7DQKThese highlights do not include all the information needed to use ABILIFY safely and effectively. See full prescribing information for ABILIFY. ABILIFY (aripiprazole) Tablets ABILIFY DISCMELT (aripiprazole) Orally Disintegrating Tablets ABILIFY (aripiprazole) Oral Solution ABILIFY (aripiprazole) Injection FOR INTRAMUSCULAR USE ONLY Initial U.S. Approval: 2002 ® ® ® ®2
FD&C BLUE NO. 2INACTIVE INGREDIENTL06K8R7DQKThese highlights do not include all the information needed to use ABILIFY safely and effectively. See full prescribing information for ABILIFY. ABILIFY (aripiprazole) Tablets ABILIFY DISCMELT (aripiprazole) Orally Disintegrating Tablets ABILIFY (aripiprazole) Oral Solution ABILIFY (aripiprazole) Injection FOR INTRAMUSCULAR USE ONLY Initial U.S. Approval: 2002 ® ® ® ®2
FD&C BLUE NO. 2INACTIVE INGREDIENTL06K8R7DQKLOSARTAN POTASSIUM TABLETS USP R x only5
FD&C BLUE NO. 2INACTIVE INGREDIENTL06K8R7DQKThese highlights do not include all the information needed to use Omeprazole delayed-release capsules safely and effectively. See full prescribing information for Omeprazole delayed-release capsules. OMEPRAZOLE delayed-release capsules, USP, for oral use Initial U.S. Approval: 198923
FD&C BLUE NO. 2INACTIVE INGREDIENTL06K8R7DQKThese highlights do not include all the information needed to use FLUOXETINE CAPSULES USP safely and effectively. See full prescribing information for FLUOXETINE CAPSULES USP. FLUOXETINE capsules USP for oral use Initial U.S. Approval: 19872
FD&C BLUE NO. 2INACTIVE INGREDIENTL06K8R7DQKThese highlights do not include all the information needed to use duloxetine delayed-release capsules safely and effectively. See full prescribing information for duloxetine delayed-release capsules. DULOXETINE delayed-release capsules for oral use. Initial U.S. Approval: 20041
FD&C BLUE NO. 2INACTIVE INGREDIENTL06K8R7DQKrOPINIRole Tablets USP1
FD&C BLUE NO. 2INACTIVE INGREDIENTL06K8R7DQK6368bb69-43e9-4304-a30d-03d593c1c05f4
FD&C BLUE NO. 2INACTIVE INGREDIENTL06K8R7DQKAMITRIPTYLINE HYDROCHLORIDE TABLETS, USP Rx only1
FD&C BLUE NO. 2INACTIVE INGREDIENTL06K8R7DQKThese highlights do not include all the information needed to use CHANTIX safely and effectively. See full prescribing information for CHANTIX. CHANTIX® (varenicline) Tablets Initial U.S. Approval: 20062
FD&C BLUE NO. 2INACTIVE INGREDIENTL06K8R7DQKThese highlights do not include all the information needed to use CHANTIX safely and effectively. See full prescribing information for CHANTIX. CHANTIX® (varenicline) Tablets Initial U.S. Approval: 20062
FD&C BLUE NO. 2INACTIVE INGREDIENTL06K8R7DQK718b6ebd-279e-4de0-ad46-c1d2a25ed19d2
FD&C BLUE NO. 2INACTIVE INGREDIENTL06K8R7DQKProbenecid Tablets, USP1
FD&C BLUE NO. 2INACTIVE INGREDIENTL06K8R7DQKbe67ff48-8e43-4589-800b-7c67d0c36cea1
FD&C BLUE NO. 2INACTIVE INGREDIENTL06K8R7DQKefbc79b9-c07c-40e3-ad8b-9bced4c93aa51
FD&C BLUE NO. 2INACTIVE INGREDIENTL06K8R7DQKDrug Facts1
FD&C BLUE NO. 2INACTIVE INGREDIENTL06K8R7DQKACETAMINOPHEN AND DIPHENHYDRAMINE HCL TABLETS1
FD&C BLUE NO. 2INACTIVE INGREDIENTL06K8R7DQKAmitriptyline Hydrochloride Tablets, USP5
FD&C BLUE NO. 2INACTIVE INGREDIENTL06K8R7DQKBuPROPion Hydrochloride Tablets, USP3
FD&C BLUE NO. 2INACTIVE INGREDIENTL06K8R7DQKBuPROPion Hydrochloride Tablets, USP3
FD&C BLUE NO. 2INACTIVE INGREDIENTL06K8R7DQKPROPRANOLOL HYDROCHLORIDE TABLETS USP Rx only1
FD&C BLUE NO. 2INACTIVE INGREDIENTL06K8R7DQKCyclobenzaprine Hydrochloride Tablets, USP5
FD&C BLUE NO. 2INACTIVE INGREDIENTL06K8R7DQKSertraline Tablets, USP 50 mg Iss. 09/12 Rx Only3
FD&C BLUE NO. 2INACTIVE INGREDIENTL06K8R7DQKThese highlights do not include all the information needed to use carvedilol safely and effectively. See full prescribing information for carvedilol tablets. Carvedilol Tablets, USP for oral use Initial U.S. Approval: 19951
FD&C BLUE NO. 2INACTIVE INGREDIENTL06K8R7DQKb32fcb1b-fee4-44b8-a91c-10dfdd3f84ea3
FD&C BLUE NO. 2INACTIVE INGREDIENTL06K8R7DQKThese highlights do not include all the information needed to use risperidone tablets safely and effectively. See full prescribing information for risperidone tablets. Risperidone Tablets USP, for oral use Initial U.S. Approval: 19933
FD&C BLUE NO. 2INACTIVE INGREDIENTL06K8R7DQKWarfarin Sodium Tablets, USP Crystalline2
FD&C BLUE NO. 2INACTIVE INGREDIENTL06K8R7DQKWarfarin Sodium Tablets, USP Crystalline2
FD&C BLUE NO. 2INACTIVE INGREDIENTL06K8R7DQKSYNTHROID® (levothyroxine sodium tablets, USP)5
FD&C BLUE NO. 2INACTIVE INGREDIENTL06K8R7DQKTamsulosin hydrochloride capsules USP, 0.4 mg These highlights do not include all the information needed to use Tamsulosin hydrochloride safely and effectively. See full prescribing information for Tamsulosin hydrochloride. Tamsulosin hydrochloride (Tamsulosin hydrochloride) CAPSULE for ORAL use. Initial U.S. Approval: 19971
FD&C BLUE NO. 2INACTIVE INGREDIENTL06K8R7DQKThese highlights do not include all the information needed to use TRIZIVIR safely and effectively. See full prescribing information for TRIZIVIR. TRIZIVIR (abacavir sulfate, lamivudine, and zidovudine) Tablets, for oral use Initial U.S. Approval: 20002
FD&C BLUE NO. 2INACTIVE INGREDIENTL06K8R7DQKAlprazolam Tablets, USP2
FD&C BLUE NO. 2INACTIVE INGREDIENTL06K8R7DQKThese highlights do not include all the information needed to use CYMBALTA safely and effectively. See full prescribing information for CYMBALTA. CYMBALTA (Duloxetine Delayed-Release Capsules) for Oral Use. Initial U.S. Approval: 20042
FD&C BLUE NO. 2INACTIVE INGREDIENTL06K8R7DQKThese highlights do not include all the information needed to use zolpidem tartrate tablets safely and effectively. See full prescribing information for zolpidem tartrate tablets Zolpidem Tartrate Tablets, for oral use CIV Initial U.S. Approval: 19922
FD&C BLUE NO. 2INACTIVE INGREDIENTL06K8R7DQKThese highlights do not include all the information needed to use ABILIFY safely and effectively. See full prescribing information for ABILIFY. ABILIFY ® (aripiprazole) Tablets ABILIFY DISCMELT ® (aripiprazole) Orally Disintegrating Tablets ABILIFY ® (aripiprazole) Oral Solution ABILIFY ® (aripiprazole) Injection FOR INTRAMUSCULAR USE ONLY Initial U.S. Approval: 20021
FD&C BLUE NO. 2INACTIVE INGREDIENTL06K8R7DQK3859effa-7b9b-41cd-9c90-847fa99e9b342
FD&C BLUE NO. 2INACTIVE INGREDIENTL06K8R7DQK4ac590e9-af71-43c0-a836-b700115d7ba22
FD&C BLUE NO. 2INACTIVE INGREDIENTL06K8R7DQKMetoprolol Tartrate Tablets USP Rx Only Prescribing Information7
FD&C BLUE NO. 2INACTIVE INGREDIENTL06K8R7DQKThese highlights do not include all the information needed to use STRIBILD safely and effectively. See full prescribing information for STRIBILD. STRIBILD ® (elvitegravir, cobicistat, emtricitabine, tenofovir disoproxil fumarate) tablets, for oral use Initial U.S. Approval: 20121
FD&C BLUE NO. 2INACTIVE INGREDIENTL06K8R7DQKSYNTHROID® (levothyroxine sodium tablets, USP)1
FD&C BLUE NO. 2INACTIVE INGREDIENTL06K8R7DQKThese highlights do not include all the information needed to use safely and effectively. See full prescribing information for . Initial U.S. Approval: 1997 budesonide capsules (enteric coated) budesonide capsules (enteric coated) BUDESONIDE capsules (enteric coated), for oral use2
FD&C BLUE NO. 2INACTIVE INGREDIENTL06K8R7DQKLOSARTAN POTASSIUM TABLETS USP R x only1
FD&C BLUE NO. 2INACTIVE INGREDIENTL06K8R7DQKDivalproex Sodium Delayed Release Tablets USP1
FD&C BLUE NO. 2INACTIVE INGREDIENTL06K8R7DQKACYCLOVIR CAPSULES USP ACYCLOVIR TABLETS USP Rx only1
FD&C BLUE NO. 2INACTIVE INGREDIENTL06K8R7DQKThese highlights do not include all the information needed to use STRATTERA safely and effectively. See full prescribing information for STRATTERA. STRATTERA (atomoxetine) CAPSULES for Oral Use Initial U.S. Approval: 2002 ®2
FD&C BLUE NO. 2INACTIVE INGREDIENTL06K8R7DQKThese highlights do not include all the information needed to use STRATTERA safely and effectively. See full prescribing information for STRATTERA. STRATTERA (atomoxetine) CAPSULES for Oral Use Initial U.S. Approval: 2002 ®2
FD&C BLUE NO. 2INACTIVE INGREDIENTL06K8R7DQKThese highlights do not include all the information needed to use STRATTERA safely and effectively. See full prescribing information for STRATTERA. STRATTERA (atomoxetine) CAPSULES for Oral Use Initial U.S. Approval: 2002 ®2
FD&C BLUE NO. 2INACTIVE INGREDIENTL06K8R7DQKThese highlights do not include all the information needed to use STRATTERA safely and effectively. See full prescribing information for STRATTERA. STRATTERA (atomoxetine) CAPSULES for Oral Use Initial U.S. Approval: 2002 ®2
FD&C BLUE NO. 2INACTIVE INGREDIENTL06K8R7DQKd4adaa46-062e-4c1e-9d9c-e7073463a40d1
FD&C BLUE NO. 2INACTIVE INGREDIENTL06K8R7DQKSERTRALINE HYDROCHLORIDE Tablets and Oral Concentrate8
FD&C BLUE NO. 2INACTIVE INGREDIENTL06K8R7DQKDoxycycline Hyclate Tablets, USP2
FD&C BLUE NO. 2INACTIVE INGREDIENTL06K8R7DQKSertraline Hydrochloride Tablets 25 mg, 50 mg and 100 mg1
FD&C BLUE NO. 2INACTIVE INGREDIENTL06K8R7DQKThese highlights do not include all the information needed to use warfarin sodium safely and effectively. See full prescribing information for warfarin sodium. Warfarin Sodium Tablets USP, for oral use Initial U.S. Approval: 19541