FDA.reportPublic FDA data

NDC 62858-101-11 - NAIL RENEW

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
62858-101
Requested NDC
62858-101-11
Package NDCs from labels
62858-101-11, 62858-101-51
Manufacturer
Nailrenew Corp
Effective date
2026-05-02
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
NAIL RENEW - Nailrenew CorpNailrenew Corp2026-05-02HUMAN OTC DRUG LABEL

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
62858-101-512019-12-31C16284748780-19855e2a2-4c9e-60a7-e053-dbdaa90a05bdNAILRENEW (62858-101)
62858-101-512019-11-27C16284748780-19855e2a2-4c9e-60a7-e053-dbdaa90a05bdNAILRENEW (62858-101)

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
62858-101-11NAIL RENEW30 mL in 1 BOTTLELIQUID309
62858-101-51NAIL RENEW1 in 1 BOXLIQUID19

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
62858-101NAIL RENEW (TOLNAFTATE) LIQUID [NAILRENEW CORP]8Current NDC, Legacy NDC, 2 package rows20240111_a0df4ee5-1276-41b7-a1c4-8fcbfc7f97b5.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
TOLNAFTATEACTIVE INGREDIENT06KB629TKVNAIL RENEW (TOLNAFTATE) LIQUID [NAILRENEW]3
TOLNAFTATEACTIVE MOIETY06KB629TKVNAIL RENEW (TOLNAFTATE) LIQUID [NAILRENEW]3
ALOE VERA LEAFINACTIVE INGREDIENTZY81Z83H0XNAIL RENEW (TOLNAFTATE) LIQUID [NAILRENEW]3
BENZYL ALCOHOLINACTIVE INGREDIENTLKG8494WBHNAIL RENEW (TOLNAFTATE) LIQUID [NAILRENEW]3
CETETH-20 PHOSPHATEINACTIVE INGREDIENT921FTA1500NAIL RENEW (TOLNAFTATE) LIQUID [NAILRENEW]3
CETOSTEARYL ALCOHOLINACTIVE INGREDIENT2DMT128M1SNAIL RENEW (TOLNAFTATE) LIQUID [NAILRENEW]3
CETYL ALCOHOLINACTIVE INGREDIENT936JST6JCNNAIL RENEW (TOLNAFTATE) LIQUID [NAILRENEW]3
COCO-BETAINEINACTIVE INGREDIENT03DH2IZ3FYNAIL RENEW (TOLNAFTATE) LIQUID [NAILRENEW]3
DIHEXADECYL PHOSPHATEINACTIVE INGREDIENT2V6E5WN99NNAIL RENEW (TOLNAFTATE) LIQUID [NAILRENEW]3
GLYCERYL MONOSTEARATEINACTIVE INGREDIENT230OU9XXE4NAIL RENEW (TOLNAFTATE) LIQUID [NAILRENEW]3
HYDROXYETHYL CELLULOSE (100 MPA.S AT 2%)INACTIVE INGREDIENTR33S7TK2EPNAIL RENEW (TOLNAFTATE) LIQUID [NAILRENEW]3
IMIDUREAINACTIVE INGREDIENTM629807ATLNAIL RENEW (TOLNAFTATE) LIQUID [NAILRENEW]3
OCTOXYNOL-9INACTIVE INGREDIENT7JPC6Y25QSNAIL RENEW (TOLNAFTATE) LIQUID [NAILRENEW]3
POLYETHYLENE GLYCOL 400INACTIVE INGREDIENTB697894SGQNAIL RENEW (TOLNAFTATE) LIQUID [NAILRENEW]3
PROPYLENE GLYCOLINACTIVE INGREDIENT6DC9Q167V3NAIL RENEW (TOLNAFTATE) LIQUID [NAILRENEW]3
PROPYLPARABENINACTIVE INGREDIENTZ8IX2SC1OHNAIL RENEW (TOLNAFTATE) LIQUID [NAILRENEW]3
STEARYL ALCOHOLINACTIVE INGREDIENT2KR89I4H1YNAIL RENEW (TOLNAFTATE) LIQUID [NAILRENEW]3
TROLAMINEINACTIVE INGREDIENT9O3K93S3TKNAIL RENEW (TOLNAFTATE) LIQUID [NAILRENEW]3
WATERINACTIVE INGREDIENT059QF0KO0RNAIL RENEW (TOLNAFTATE) LIQUID [NAILRENEW]3

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 65 of 68 · 1,357 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
Povidone IodinePOVIDONE-IODINEDr Radows58e1757c-45ce-455e-bd64-a9e99cd3680f2023-10-30WarningsExact identifier
application number: M005
JOCK-EZECLOTRIMAZOLEBentlin Products LLCd3ff5bfb-2e0f-4daa-84b3-4a3016ca92802023-10-30WarningsExact identifier
application number: M005
TheraPlus PlusCLOTRIMAZOLEZhejiang Jingwei Pharmaceutical Co., Ltd.de75179d-1889-4823-9f39-4bebdf185d762023-10-27WarningsExact identifier
application number: M005
Evercare Antifungal Treatment Super Absorbent PowderMICONAZOLE NITRATEPANEFFORT, LLCf91910f3-b461-43a4-9120-fda69483fffa2023-10-26WarningsExact identifier
application number: M005
Thera plus Antifungal ClotrimazoleCLOTRIMAZOLEFOURSTAR GROUP USA, INC.1265be99-8922-4b76-bd63-19bfb42c38962023-10-26WarningsExact identifier
application number: M005
Thera plus Antifungal TolnaftateTOLNAFTATEFOURSTAR GROUP USA, INC.c628dda8-7a6d-5f3a-e053-2995a90a35f82023-10-26WarningsExact identifier
application number: M005
unii: 06KB629TKV
Povidone IodinePOVIDONE IODINEJianerkang Medical Co., Ltde1789944-3a41-4c86-b173-3a6993ae21412023-10-23WarningsExact identifier
application number: M005
Povidone Iodine ImpregnatedPOVIDONE IODINEJianerkang Medical Co., Ltd14f2a1dd-92c2-49e8-9fa0-a9d88e8c530d2023-10-23WarningsExact identifier
application number: M005
Povidone Iodine ImpregnatedPOVIDONE IODINEJianerkang Medical Co., Ltdb82cea56-b09f-411d-a6cf-c53b3ce0e3b62023-10-23WarningsExact identifier
application number: M005
Povidone Iodine ScrubPOVIDONE-IODINEJianerkang Medical Co., Ltd78131b57-1ffc-4eb8-821e-f7bb73300fe92023-10-23WarningsExact identifier
application number: M005
Povidone IodinePOVIDONE IODINEJianerkang Medical Co., Ltdeb30e5de-9074-4760-8e92-e1d1c127227d2023-10-23WarningsExact identifier
application number: M005
Povidone IodinePOVIDONE IODINEJianerkang Medical Co., Ltd0bd3de76-b726-41f1-87bc-14ab8a1eca8e2023-10-23WarningsExact identifier
application number: M005
Povidone Iodine Prep PadPOVIDONE-IODINEJianerkang Medical Co., Ltdbe85ec5b-eb49-4f1a-a87d-5c9705a20f232023-10-22WarningsExact identifier
application number: M005
Mycozyl ALTOLNAFTATEPURETEK CORPORATION07edd043-4ac4-b2de-e063-6394a90af25d2023-10-17Warnings, Adverse reactionsExact identifier
rxcui: 313423
unii: 06KB629TKV
EVERLIT CARE Hand SanitizerETHYL ALCOHOLNantong Health & Beyond Hygienic Products Inc.579c1ab5-50b4-4b5a-a189-c1e2827d0c3a2023-10-14WarningsExact identifier
application number: M005
ANUBISMEDHA HYALURONICANUBIS COSMETICS SLeac771e2-4c1b-3808-e053-2995a90ac5fc2023-09-05WarningsExact identifier
unii: 6DC9Q167V3
unii: 9O3K93S3TK
unii: ZY81Z83H0X
unii: 059QF0KO0R
unii: 936JST6JCN
unii: M629807ATL
unii: 230OU9XXE4
AnubisMedSPF 50 BROAD SPECTRUM PROTECTION FLUID EMULSIONANUBIS COSMETICS SLe99d92c4-8768-9c0a-e053-2a95a90a609e2023-09-05WarningsExact identifier
unii: 6DC9Q167V3
unii: B697894SGQ
unii: 059QF0KO0R
AnubisMedAZELAIC ACID, SALICYLIC ACIDANUBIS COSMETICS SLebf3153d-30f5-54e4-e053-2995a90a74b12023-09-05WarningsExact identifier
unii: 6DC9Q167V3
unii: B697894SGQ
unii: 059QF0KO0R
AnubisMedGLYCOLIC ACID, CITRIC ACID, LACTIC ACID, KOJIC ACIDANUBIS COSMETICS SLeca95dde-cb57-2ab6-e053-2995a90af84f2023-09-05WarningsExact identifier
unii: 6DC9Q167V3
unii: 059QF0KO0R
AnubisMedSODIUM BICARBONATE, ALOE BARBADENSIS LEAF JUICE, IMIDAZOLIDINYL UREAANUBIS COSMETICS SLebf4b3ab-34e1-185a-e053-2a95a90ace3a2023-09-05WarningsExact identifier
unii: ZY81Z83H0X
unii: 059QF0KO0R
unii: M629807ATL

Reported adverse events (FAERS/openFDA)#

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