FDA.reportPublic FDA data

lemon and shea butter

Manufacturer
Jack Black L.L.C. | Raining Rose
Effective date
2026-02-25
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 01:52:33

Label at a glance#

ProductJack Black
Active ingredientHOMOSALATE, OCTISALATE, AVOBENZONE, PETROLATUM
Label structure9 sections

Dosage and administration

• Apply liberally before sun exposure and reapply every 2 hours.

Label contents#

Full prescribing information#

Active ingredients

OTC - ACTIVE INGREDIENT SECTION

Avobenzone 3%

Homosalate 10%

Octisalate 5%

Petrolatum 40.2%

Purposes

OTC - PURPOSE SECTION

Sunscreen

Sunscreen

Sunscreen

Skin protectant

Use

INDICATIONS & USAGE SECTION

• Helps protect against sunburn and chapped lips.

Warning

WARNINGS SECTION

Stop use if skin rash occurs.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children.

Directions

DOSAGE & ADMINISTRATION SECTION

• Apply liberally before sun exposure and reapply every 2 hours.

Inactive ingredients

INACTIVE INGREDIENT SECTION

Beeswax, Ozokerite, Polyglyceryl-3 Beeswax, Butyloctyl Salicylate, Polypinene, Ethylhexyl Methoxycrylene, Hydrogenated Soybean Oil, Hydrogenated Coconut Oil, Fragrance, Theobroma Cacao (Cocoa) Seed Butter, Synthetic Beeswax, Cetyl Alcohol, Euphorbia Cerifera (Candelilla) Wax, Butyrospermum Parkii (Shea) Butter, Persea Gratissima (Avocado) Oil, Tocopheryl Acetate, Lecithin, Helianthus Annuus (Sunflower) Seed Oil, Microcrystalline Wax, Camellia Sinensis Leaf Extract

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

PDPPDP

Product Linked Resources#

Resource, Code type, Value table
ResourceCode typeValueEquivalent identifiersSource image
BarcodeEAN-130682223030103GTIN-13: 0682223030103
EAN-13: 0682223030103
GTIN-12: 682223030103
UPC-A: 682223030103
GTIN storage (14 digits): 00682223030103		lemon and shea.jpg

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
66738-791-01Jack Black1 in 1 CARTONOINTMENT11
66738-791-21Jack Black7 mL in 1 TUBEOINTMENT71

Products#

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

DailyMed product names page 1 of 1 · 22 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
66738-79166738-791-21, 66738-791-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 20 matching rows.

Name, UNII, Kind table
NameUNIIKind
HOMOSALATEV06SV4M95SACTIB
POLYGLYCERYL-3 BEESWAXZ98M8HW9A6IACT
OCTISALATE4X49Y0596WACTIB
BEESWAX2ZA36H0S2VIACT
THEOBROMA CACAO (COCOA) SEED BUTTER512OYT1CRRIACT
SYNTHETIC BEESWAX08MNR5YE2RIACT
HYDROGENATED COCONUT OILJY81OXM1OMIACT
BUTYLOCTYL SALICYLATE2EH13UN8D3IACT
PERSEA GRATISSIMA (AVOCADO) OIL6VNO72PFC1IACT
.ALPHA.-TOCOPHEROL ACETATE9E8X80D2L0IACT
ETHYLHEXYL METHOXYCRYLENES3KFG6Q5X8IACT
CAMELLIA SINENSIS LEAFW2ZU1RY8B0IACT
HELIANTHUS ANNUUS (SUNFLOWER) SEED OIL3W1JG795YIIACT
HYDROGENATED SOYBEAN OILA2M91M918CIACT
CETYL ALCOHOL936JST6JCNIACT
BUTYROSPERMUM PARKII (SHEA) BUTTERK49155WL9YIACT
AVOBENZONEG63QQF2NOXACTIB
MICROCRYSTALLINE WAXXOF597Q3KYIACT
EUPHORBIA CERIFERA (CANDELILLA) WAXWL0328HX19IACT
PETROLATUM4T6H12BN9UACTIB

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
Jack BlackAVOBENZONE/HOMOSALATE/OCTISALATE/PETROLATUMJack Black L.L.C.4bac5550-c45f-a738-e063-6394a90ae5c82026-02-25WarningsExact identifier
ndc (package): 66738-791-01
ndc (package): 66738-791-21
ndc (product): 66738-791
ndc11 (package): 66738079121
ndc11 (package): 66738079101
spl id: 4bac5550-c460-a738-e063-6394a90ae5c8
spl set id: 4bac5550-c45f-a738-e063-6394a90ae5c8

Reported adverse events (FAERS/openFDA)#

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