FDA.reportPublic FDA data

Blistex Deep Renewal International

Manufacturer
Blistex Inc.
Effective date
2016-04-29
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 22:45:51

Label at a glance#

ProductBlistex Deep Renewal International
Active ingredientDIMETHICONE, OCTINOXATE, OXYBENZONE
Label structure1 sections

Label contents#

Full prescribing information#

PRINCIPAL DISPLAY PANEL - 3.69 g Cylinder Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Blistex®
Lip Protector

PRINCIPAL DISPLAY PANEL - 3.69 g Cylinder Label
PRINCIPAL DISPLAY PANEL - 3.69 g Cylinder Label

DailyMed Pharmacologic Classes#

Class, Version, Type table
ClassVersionTypeEffective
DIMETHICONE Pharmacologic Class Indexing3Indexing - Pharmacologic Class20180813

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
10157-9836-12020-01-31C16284748780-19d75b9cf-f374-f424-e053-dadaa90a57ceBlistex ® Deep Renewal International

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
10157-9836-1Blistex Deep Renewal International3.69 g in 1 CYLINDERSTICK3.691

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
10157-9836BLISTEX DEEP RENEWAL INTERNATIONAL (DIMETHICONE, OCTINOXATE, AND OXYBENZONE) STICK [BLISTEX INC.]11 package rows20160503_cf6efea6-2db0-4d0e-b35b-745bc654ab65.zip

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 30 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
10157-983610157-9836-1

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 28 matching rows.

Name, UNII, Kind table
NameUNIIKind
DIMETHICONE92RU3N3Y1OACTIB
OCTINOXATE4Y5P7MUD51ACTIB
OXYBENZONE95OOS7VE0YACTIB
OCTYLDODECANOL461N1O614YIACT
Hydrogenated jojoba oil, randomizedQ47ST02F58IACT
MICROCRYSTALLINE WAXXOF597Q3KYIACT
PETROLATUM4T6H12BN9UIACT
CASTOR OILD5340Y2I9GIACT
YELLOW WAX2ZA36H0S2VIACT
POLYBUTENE (1400 MW)1NA5AO9GH7IACT
HIGH DENSITY POLYETHYLENEUG00KM4WR7IACT
POLYTETRAFLUOROETHYLENEE1NC1JVS3OIACT
ETHYLHEXYL PALMITATE2865993309IACT
SILICA DIMETHYL SILYLATEEU2PSP0G0WIACT
BUTYLENE GLYCOL3XUS85K0RAIACT
HYALURONATE SODIUMYSE9PPT4THIACT
SQUALANEGW89575KF9IACT
DIPALMITOYL HYDROXYPROLINEE6AHA53N1HIACT
.ALPHA.-TOCOPHEROL ACETATE9E8X80D2L0IACT
LANOLIN ALCOHOLS884C3FA9HEIACT
PENTAERYTHRITYL TETRAISOSTEARATE9D7IK5483FIACT
CHONDROITIN SULFATE SODIUM (SHARK)Q75WVO004LIACT
MARINE COLLAGEN, SOLUBLE8JC99XGU4WIACT
TETRAHEXYLDECYL ASCORBATE9LBV3F07AZIACT
PHENOXYETHANOLHIE492ZZ3TIACT
SACCHARINFST467XS7DIACT
SORBIC ACIDX045WJ989BIACT
UBIDECARENONEEJ27X76M46IACT

Source Document#

Source XML

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 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
21a319cc-02fe-42a0-bf8e-193ea9a60483cf6efea6-2db0-4d0e-b35b-745bc654ab652016-04-29Exact identifier
spl id: 21a319cc-02fe-42a0-bf8e-193ea9a60483
spl set id: cf6efea6-2db0-4d0e-b35b-745bc654ab65

Reported adverse events (FAERS/openFDA)#

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