FDA.reportPublic FDA data

LIP BALM

Manufacturer
Private Label Select Ltd CO
Effective date
2020-12-30
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:36:13

Label at a glance#

ProductLIP BALM
Active ingredientOXYBENZONE, OCTINOXATE, AVOBENZONE
Label structure5 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

OTC Active IngredientsOTC Active Ingredients

OTC - KEEP OUT OF REACH OF CHILDREN

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

OTC Keep Out Of Reach Of ChildrenOTC Keep Out Of Reach Of Children

OTC - PURPOSE

OTC - PURPOSE SECTION

OTC PurposeOTC Purpose

ARTWORK (INSIDE)

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

ArtworkArtwork

ARTWORK (OUTSIDE)

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

ArtworkArtwork

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
62932-236-382022-01-28C16284748780-1d6a99b39-e8b8-a426-e053-dadaa90af4c2Napa Soap Mimosa SPF 15 Natural Lip Balm

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
62932-236-38LIP BALM4.25 g in 1 CONTAINERSTICK4.251

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
62932-236LIP BALM (SUNSCREEN LIP BALM) STICK [PRIVATE LABEL SELECT LTD CO]1Legacy NDC, 1 package rows20201231_b7b252da-9d1d-0bf5-e053-2a95a90aaec8.zip

Products#

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

DailyMed product names page 1 of 1 · 18 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
62932-23662932-236-38

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 16 matching rows.

Name, UNII, Kind table
NameUNIIKind
SUNFLOWER OIL3W1JG795YIIACT
WHITE WAX7G1J5DA97FIACT
OXYBENZONE95OOS7VE0YACTIB
OCTINOXATE4Y5P7MUD51ACTIB
AVOBENZONEG63QQF2NOXACTIB
GRAPE SEED OIL930MLC8XGGIACT
COCONUT OILQ9L0O73W7LIACT
SHEA BUTTERK49155WL9YIACT
.ALPHA.-TOCOPHEROL, D-N9PR3490H9IACT
RESVERATROLQ369O8926LIACT
TANGERINEKH3E3096OOIACT
.BETA.-TOCOPHEROL9U6A490501IACT
.DELTA.-TOCOPHEROLJU84X1II0NIACT
.GAMMA.-TOCOPHEROL8EF1Z1238FIACT
AMMONIUM GLYCYRRHIZATE3VRD35U26CIACT
ORANGE OILAKN3KSD11BIACT

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
b7b252da-9d1e-0bf5-e053-2a95a90aaec8b7b252da-9d1d-0bf5-e053-2a95a90aaec82020-12-30Exact identifier
spl id: b7b252da-9d1e-0bf5-e053-2a95a90aaec8
spl set id: b7b252da-9d1d-0bf5-e053-2a95a90aaec8

Reported adverse events (FAERS/openFDA)#

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