LypSyl Honeyberry

Manufacturer
Lornamead
Effective date
2018-12-27
Label type
HUMAN OTC DRUG LABEL
Version
5
Source
full-release
Hydrated at
2026-05-31 22:57:59

Label at a glance#

ProductLypSyl Honeyberry
Active ingredientOCTINOXATE, OCTOCRYLENE, OXYBENZONE
Label structure8 sections

Dosage and administration

Apply liberally before sun exposure and as needed children under 6 months of age: ask a doctor

Label contents#

Full prescribing information#

Active ingredients

OTC - ACTIVE INGREDIENT SECTION

Octyl Methoxycinnamate 5.5%
Octocrylene 2.0%
Oxybenzone 3.5%

Use

OTC - PURPOSE SECTION

Sunscreen

WARNINGS SECTION

Stop use and ask a doctor -

if rash or irritation develops and lasts

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control

Center right away.

Directions

INDICATIONS & USAGE SECTION

Apply liberally before sun exposure and as needed

children under 6 months of age:

ask a doctor

Questions or Comments

OTHER SAFETY INFORMATION

Call 1-877-995-5405 or email customerservice@lornameadna.com - www.lypsylhome.com

Inactive ingredients

INACTIVE INGREDIENT SECTION

Beeswax, Persea Gratissima (Avocado), Butter, Butyrospermum Parkii (Shea Butter), Simmondsia,
Chinensis (Jojoba) Seed Oil, Flavor, Tocopheryl Acetate (Vitamin E Acetate), Retinyl Palmitate (Vitamin A Palmitate)

DOSAGE & ADMINISTRATION SECTION

Apply liberally before sun exposure and as needed

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Carton label
Carton label

Cylinder label
Cylinder label


FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
62721-8106-82020-01-31C16284748780-19d75b9d0-7495-f424-e053-dadaa90a57ceDrug Facts

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
62721-8106-6LypSyl Honeyberry2.83 g in 1 CANISTERLIPSTICK2.835
62721-8106-8LypSyl Honeyberry1 in 1 BLISTER PACKLIPSTICK15

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
62721-8106LYPSYL HONEYBERRY (OCTINOXATE) LIPSTICK [LORNAMEAD]5Legacy NDC, 2 package rows20181228_998d0c46-1256-495f-81d9-65959dd6414d.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
OCTINOXATEACTIVE INGREDIENT4Y5P7MUD514
OCTOCRYLENEACTIVE INGREDIENT5A68WGF6WM4
OXYBENZONEACTIVE INGREDIENT95OOS7VE0Y4
OCTINOXATEACTIVE MOIETY4Y5P7MUD514
OCTOCRYLENEACTIVE MOIETY5A68WGF6WM4
OXYBENZONEACTIVE MOIETY95OOS7VE0Y4
ALPHA-TOCOPHEROLINACTIVE INGREDIENTH4N855PNZ14
JOJOBA OILINACTIVE INGREDIENT724GKU717M4
PERSEA AMERICANA SEED BUTTERINACTIVE INGREDIENTTSD0N1V8MB4
SHEA BUTTERINACTIVE INGREDIENTK49155WL9Y4
VITAMIN A PALMITATEINACTIVE INGREDIENT1D1K0N0VVC4
YELLOW WAXINACTIVE INGREDIENT2ZA36H0S2V4

Products#

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

DailyMed product names page 1 of 1 · 10 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
62721-810662721-8106-6, 62721-8106-8

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 9 matching rows.

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 · 20 matching rows.

DailyMed ingredient, IID ingredient, UNII table
DailyMed ingredientIID ingredientUNIIDosage form / routePotencyMaximum daily exposureMatch
ALPHA-TOCOPHEROL.ALPHA.-TOCOPHEROLH4N855PNZ1CAPSULE / ORAL16 mgExact identifier — unii candidate
10 equally ranked IID candidates
ALPHA-TOCOPHEROL.ALPHA.-TOCOPHEROLH4N855PNZ1SOLUTION / ORAL1.05 mg/1mlExact identifier — unii candidate
10 equally ranked IID candidates
ALPHA-TOCOPHEROL.ALPHA.-TOCOPHEROLH4N855PNZ1SYSTEM / TOPICAL0.1 mgExact identifier — unii candidate
10 equally ranked IID candidates
ALPHA-TOCOPHEROL.ALPHA.-TOCOPHEROLH4N855PNZ1TABLET, EXTENDED RELEASE / ORAL4 mgExact identifier — unii candidate
10 equally ranked IID candidates
YELLOW WAXYELLOW WAX2ZA36H0S2VOINTMENT / TOPICAL357 mgExact identifier — unii candidate
9 equally ranked IID candidates
ALPHA-TOCOPHEROL.ALPHA.-TOCOPHEROLH4N855PNZ1FILM, SOLUBLE / BUCCAL0.07 mgExact identifier — unii candidate
10 equally ranked IID candidates
ALPHA-TOCOPHEROL.ALPHA.-TOCOPHEROLH4N855PNZ1TABLET, CHEWABLE / ORAL0.1 mgExact identifier — unii candidate
10 equally ranked IID candidates
ALPHA-TOCOPHEROL.ALPHA.-TOCOPHEROLH4N855PNZ1OINTMENT / TOPICALNAExact identifier — unii candidate
10 equally ranked IID candidates
YELLOW WAXYELLOW WAX2ZA36H0S2VCREAM / TOPICAL5 %w/wExact identifier — unii candidate
9 equally ranked IID candidates
YELLOW WAXYELLOW WAX2ZA36H0S2VTABLET, SUGAR COATED / ORALNAExact identifier — unii candidate
9 equally ranked IID candidates
ALPHA-TOCOPHEROL.ALPHA.-TOCOPHEROLH4N855PNZ1TABLET / ORAL2 mgExact identifier — unii candidate
10 equally ranked IID candidates
YELLOW WAXYELLOW WAX2ZA36H0S2VTABLET, DELAYED RELEASE / ORAL0.1 mgExact identifier — unii candidate
9 equally ranked IID candidates
ALPHA-TOCOPHEROL.ALPHA.-TOCOPHEROLH4N855PNZ1TABLET, FILM COATED / ORAL246 mgExact identifier — unii candidate
10 equally ranked IID candidates
SHEA BUTTERSHEA BUTTERK49155WL9YLOTION / TOPICAL2340 mgExact identifier — unii candidate
YELLOW WAXYELLOW WAX2ZA36H0S2VCAPSULE / ORAL44 mgExact identifier — unii candidate
9 equally ranked IID candidates
ALPHA-TOCOPHEROL.ALPHA.-TOCOPHEROLH4N855PNZ1INJECTION, POWDER, FOR SUSPENSION / INTRAVENOUS0.64 mgExact identifier — unii candidate
10 equally ranked IID candidates
YELLOW WAXYELLOW WAX2ZA36H0S2VTABLET, COATED / ORAL213.7 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
YELLOW WAXYELLOW WAX2ZA36H0S2VTABLET, EXTENDED RELEASE / ORAL0.01 mgExact identifier — unii candidate
9 equally ranked IID candidates
YELLOW WAXYELLOW WAX2ZA36H0S2VTABLET / ORAL3.22 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
7e03a6b4-2331-2b97-e053-2991aa0a4d70998d0c46-1256-495f-81d9-65959dd6414d2018-12-27WarningsExact identifier
spl id: 7e03a6b4-2331-2b97-e053-2991aa0a4d70
spl set id: 998d0c46-1256-495f-81d9-65959dd6414d

Reported adverse events (FAERS/openFDA)#

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