FDA.reportPublic FDA data

Aunt Bees Five Flavors

Manufacturer
Private Label Select | Private Label Select, LLC
Effective date
2015-03-12
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
full-release
Hydrated at
2026-05-31 22:41:58

Label at a glance#

ProductAunt Bees Five Flavors Wintermint Lip Balm
Active ingredientOCTINOXATE, OCTISALATE, OXYBENZONE, AVOBENZONE
Label structure3 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Active Ingredients:  Octinoxate, Octyl Salicylate, Oxybenzone, Avobenzone.  

INACTIVE INGREDIENT SECTION

Contains:  *Sunflower Oil (Helianthus annuus), *Beeswax (Cera alba), *Jojoba Oil (Simmondsia chimensis), *Flavors, Tocopherol (non GMO), *Aloe Vera (Aloe barbadensis) *Organic

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Aunt Bee's5flavors tm

(flavor) balm

net wt. 15 oz (4.2g)

Made in USA in a Certified Organic facility (NM Organic Commodity Commission)

PO Box 2678 Ranchos de Taos NM 87557

www.auntbeesskincare.com  1.888.BEE.BALM

5-80189-00100-6 (UPC)


Wintermint Lip BalmWintermint Lip Balm

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
62932-146-252020-01-31C16284748780-19d75b9cf-d742-f424-e053-dadaa90a57ceLabel Data

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
62932-146-25Aunt Bees Five FlavorsWintermint Lip Balm4.2 g in 1 TUBESALVE4.23

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
62932-146AUNT BEES FIVE FLAVORS WINTERMINT LIP BALM (LIP BALM SPF 35) SALVE [PRIVATE LABEL SELECT]3Legacy NDC, 1 package rows20150313_f188d14a-8a67-4235-9b3c-a385e48a779d.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
AVOBENZONEACTIVE INGREDIENTG63QQF2NOX3
OCTINOXATEACTIVE INGREDIENT4Y5P7MUD513
OCTISALATEACTIVE INGREDIENT4X49Y0596W3
OXYBENZONEACTIVE INGREDIENT95OOS7VE0Y3
AVOBENZONEACTIVE MOIETYG63QQF2NOX3
OCTINOXATEACTIVE MOIETY4Y5P7MUD513
OCTISALATEACTIVE MOIETY4X49Y0596W3
OXYBENZONEACTIVE MOIETY95OOS7VE0Y3
Yellow WaxINACTIVE INGREDIENT2ZA36H0S2V3

Products#

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

DailyMed product names page 1 of 1 · 7 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
62932-14662932-146-25

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 5 matching rows.

Name, UNII, Kind table
NameUNIIKind
Yellow Wax2ZA36H0S2VIACT
OCTINOXATE4Y5P7MUD51ACTIB
OCTISALATE4X49Y0596WACTIB
OXYBENZONE95OOS7VE0YACTIB
AVOBENZONEG63QQF2NOXACTIB

Source Document#

Source XML

Inactive ingredient matches#

Inactive Ingredient Database values describe FDA-listed use contexts. The match method and ambiguity count are shown because ingredient names, routes, and dosage forms are not always unique. Browse recovered IID releases and source provenance.

Inactive ingredient links page 1 of 1 · 9 matching rows.

DailyMed ingredient, IID ingredient, UNII table
DailyMed ingredientIID ingredientUNIIDosage form / routePotencyMaximum daily exposureMatch
Yellow WaxYELLOW WAX2ZA36H0S2VTABLET, EXTENDED RELEASE / ORAL0.01 mgExact identifier — unii candidate
9 equally ranked IID candidates
Yellow WaxYELLOW WAX2ZA36H0S2VTABLET, DELAYED RELEASE / ORAL0.1 mgExact identifier — unii candidate
9 equally ranked IID candidates
Yellow WaxYELLOW WAX2ZA36H0S2VTABLET, SUGAR COATED / ORALNAExact identifier — unii candidate
9 equally ranked IID candidates
Yellow WaxYELLOW WAX2ZA36H0S2VCREAM / TOPICAL5 %w/wExact identifier — unii candidate
9 equally ranked IID candidates
Yellow WaxYELLOW WAX2ZA36H0S2VCAPSULE / ORAL44 mgExact identifier — unii candidate
9 equally ranked IID candidates
Yellow WaxYELLOW WAX2ZA36H0S2VTABLET, COATED / ORAL213.7 mgExact identifier — unii candidate
9 equally ranked IID candidates
Yellow WaxYELLOW WAX2ZA36H0S2VOINTMENT / TOPICAL20 %w/wExact identifier — unii candidate
9 equally ranked IID candidates
Yellow WaxYELLOW WAX2ZA36H0S2VTABLET / ORAL3.22 mgExact identifier — unii candidate
9 equally ranked IID candidates
Yellow WaxYELLOW WAX2ZA36H0S2VCAPSULE, EXTENDED RELEASE / ORAL80.67 mgExact identifier — unii candidate
9 equally ranked IID candidates

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
111c9156-2828-1694-e054-00144ff8d46cf188d14a-8a67-4235-9b3c-a385e48a779d2015-03-12Exact identifier
spl id: 111c9156-2828-1694-e054-00144ff8d46c
spl set id: f188d14a-8a67-4235-9b3c-a385e48a779d

Reported adverse events (FAERS/openFDA)#

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