EQUALINE

Product NDC
41163-618
11-digit product format
411630618
Labeler code
41163
Product ID
41163-618_990ce740-8c8f-40bd-aa96-6d60a1eff961
Type
HUMAN OTC DRUG
Nonproprietary name
SELENIUM SULFIDE
Dosage form
LIQUID
Route
TOPICAL
Labeler
SUPERVALU INC.
Application
part358H
Marketing category
OTC MONOGRAPH FINAL
Marketing start
2013-02-14
Marketing end
0000-00-00
Substance
SELENIUM SULFIDE
Active strength
10 mg/mL
NDC exclude flag
No
Listing certified through
2019-12-31
Current FDA listing
Historical FDA.report record

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
362d7abb-94e6-4c60-9a58-266894157713Product name120231023
6bd95106-a412-1dad-b9cc-4cb74bfb27ceProduct name220230315
c6f86816-7da6-43ea-8c25-ac9758311cc5Product name120220118
f1e0dc7e-7d61-4625-b6d9-4894927679d7Product name220211025
e4870509-7e28-6f92-f0be-dd3dd889a9cfProduct name520200810
6e9d4a47-c464-b93e-aebc-ad7bffc9c4cdProduct name220190619
444b3e50-f226-46ef-bfca-2e7035d140cdProduct name120190611
816b97af-edc5-4060-aff1-b814bdbcad50Product name120190415
7cda52fc-125f-421c-8fea-bc1974370c49Product name220180703
252e11b6-1a9a-4283-a242-df2c129c496dProduct name320170717
419aab54-5d5a-4146-9453-026d4a9991beProduct name220170525
d5e51f11-ad28-caa4-4b49-4143974782adProduct name120150831
290f523a-f9db-9774-b5a9-e1f908ac1782Product name120150828
89dac932-b90a-4410-9ab1-84c53e57de25Product name120150316
5668b646-cd56-c3c7-bdea-3f6b1a8840dbProduct name120140508
684ea482-2e8b-14af-5664-b98f1e402036Product name120140508
810ab97e-f109-f41c-7c83-6a652a9cbf43Product name120140508
87711080-88eb-65c5-b2dd-bf99e700a372Product name120140508
8dbefedf-0a0d-a224-5a3c-66dc9e11c2ddProduct name120140508
b060cc1a-fe47-856b-0b77-4448b5963de8Product name120140508
c6b65c52-69c7-df49-550a-a50c137f6218Product name120140508
ec2149b3-5c6d-5344-f757-c86411073075Product name120140508
ed912195-5da0-0f2f-6f4b-3ef17710cbe3Product name120140508

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
41163-618-142020-01-31C16284748780-19d75b9d1-0ba6-f424-e053-dadaa90a57ceDRUG FACTS

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
41163-618-14EQUALINECLINICAL STRENGTH420 mL in 1 BOTTLE, PLASTICLIQUID4201

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
SELENIUM SULFIDEACTIVE INGREDIENTZ69D9E381QEQUALINE CLINICAL STRENGTH (SELENIUM SULFIDE) LIQUID [SUPERVALU INC.]1
SELENIUM SULFIDEACTIVE MOIETYZ69D9E381QEQUALINE CLINICAL STRENGTH (SELENIUM SULFIDE) LIQUID [SUPERVALU INC.]1
AMMONIUM LAURETH-3 SULFATEINACTIVE INGREDIENT896SJ235FNEQUALINE CLINICAL STRENGTH (SELENIUM SULFIDE) LIQUID [SUPERVALU INC.]1
AMMONIUM LAURYL SULFATEINACTIVE INGREDIENTQ7AO2R1M0BEQUALINE CLINICAL STRENGTH (SELENIUM SULFIDE) LIQUID [SUPERVALU INC.]1
AMMONIUM XYLENESULFONATEINACTIVE INGREDIENT4FZY6L6XCMEQUALINE CLINICAL STRENGTH (SELENIUM SULFIDE) LIQUID [SUPERVALU INC.]1
CETYL ALCOHOLINACTIVE INGREDIENT936JST6JCNEQUALINE CLINICAL STRENGTH (SELENIUM SULFIDE) LIQUID [SUPERVALU INC.]1
CITRIC ACID MONOHYDRATEINACTIVE INGREDIENT2968PHW8QPEQUALINE CLINICAL STRENGTH (SELENIUM SULFIDE) LIQUID [SUPERVALU INC.]1
COCO MONOETHANOLAMIDEINACTIVE INGREDIENTC80684146DEQUALINE CLINICAL STRENGTH (SELENIUM SULFIDE) LIQUID [SUPERVALU INC.]1
DIMETHICONEINACTIVE INGREDIENT92RU3N3Y1OEQUALINE CLINICAL STRENGTH (SELENIUM SULFIDE) LIQUID [SUPERVALU INC.]1
EDETATE DISODIUMINACTIVE INGREDIENT7FLD91C86KEQUALINE CLINICAL STRENGTH (SELENIUM SULFIDE) LIQUID [SUPERVALU INC.]1
FD&C RED NO. 4INACTIVE INGREDIENTX3W0AM1JLXEQUALINE CLINICAL STRENGTH (SELENIUM SULFIDE) LIQUID [SUPERVALU INC.]1
GLYCOL DISTEARATEINACTIVE INGREDIENT13W7MDN21WEQUALINE CLINICAL STRENGTH (SELENIUM SULFIDE) LIQUID [SUPERVALU INC.]1
HYPROMELLOSESINACTIVE INGREDIENT3NXW29V3WOEQUALINE CLINICAL STRENGTH (SELENIUM SULFIDE) LIQUID [SUPERVALU INC.]1
METHACRYLIC ACID - METHYL METHACRYLATE COPOLYMER (1:1)INACTIVE INGREDIENT74G4R6TH13EQUALINE CLINICAL STRENGTH (SELENIUM SULFIDE) LIQUID [SUPERVALU INC.]1
METHYLCHLOROISOTHIAZOLINONEINACTIVE INGREDIENTDEL7T5QRPNEQUALINE CLINICAL STRENGTH (SELENIUM SULFIDE) LIQUID [SUPERVALU INC.]1
METHYLISOTHIAZOLINONEINACTIVE INGREDIENT229D0E1QFAEQUALINE CLINICAL STRENGTH (SELENIUM SULFIDE) LIQUID [SUPERVALU INC.]1
SODIUM BENZOATEINACTIVE INGREDIENTOJ245FE5EUEQUALINE CLINICAL STRENGTH (SELENIUM SULFIDE) LIQUID [SUPERVALU INC.]1
SODIUM CHLORIDEINACTIVE INGREDIENT451W47IQ8XEQUALINE CLINICAL STRENGTH (SELENIUM SULFIDE) LIQUID [SUPERVALU INC.]1
SODIUM CITRATEINACTIVE INGREDIENT1Q73Q2JULREQUALINE CLINICAL STRENGTH (SELENIUM SULFIDE) LIQUID [SUPERVALU INC.]1
STEARYL ALCOHOLINACTIVE INGREDIENT2KR89I4H1YEQUALINE CLINICAL STRENGTH (SELENIUM SULFIDE) LIQUID [SUPERVALU INC.]1
WATERINACTIVE INGREDIENT059QF0KO0REQUALINE CLINICAL STRENGTH (SELENIUM SULFIDE) LIQUID [SUPERVALU INC.]1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
41163-618EQUALINE CLINICAL STRENGTH (SELENIUM SULFIDE) LIQUID [SUPERVALU INC.]1Legacy NDC, 1 package rows20130214_1e03fd8b-c18f-43c3-9527-8746f5abddc5.zip

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
204642selenium sulfide 1 % Medicated ShampooPSN1e03fd8b-c18f-43c3-9527-8746f5abddc51
204642selenium sulfide 10 MG/ML Medicated ShampooSCD1e03fd8b-c18f-43c3-9527-8746f5abddc51
204642selenium sulfide 1 % Lotion ShampooSY1e03fd8b-c18f-43c3-9527-8746f5abddc51
204642selenium sulfide 1 % Medicated ShampooSY1e03fd8b-c18f-43c3-9527-8746f5abddc51

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsStatus
41163-618-1441163061814420 mL in 1 BOTTLE, PLASTIC420 mlHistorical