FDA.reportPublic FDA data

Jack Black Double Duty

Manufacturer
Jack Black L.L.C.
Effective date
2025-08-27
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-06-01 01:11:57

Label at a glance#

ProductJack Black Double Duty
Active ingredientOCTOCRYLENE, AVOBENZONE
Label structure9 sections

Indications and uses

Helps prevent sunburn.

Dosage and administration

• Apply liberally 15 minutes before sun exposure. • children under 6 months: Ask a doctor • reapply at least every 2 hours • use a water resistant sunscreen if swimming or sweating. • Sun Protection Measures: Spending time in the sun increases your risk of skin cancer and early skin aging. To decrease this risk, regularly use sunscreen with a broad-spectrum SPF value of 15 or higher. • Limit time in the sun, espec...

Storage and handling

• protect the product in this container from excessive heat and direct sun

Label contents#

Full prescribing information#

Active Ingredients

OTC - ACTIVE INGREDIENT SECTION

Avobenzone 2.2%

Octocrylene 9.5%

Purpose

OTC - PURPOSE SECTION

Sunscreen

Uses

INDICATIONS & USAGE SECTION

Helps prevent sunburn.

Warnings

WARNINGS SECTION

For external use only

Do not use

OTC - DO NOT USE SECTION

• on damaged or broken skin

When using this product

OTC - WHEN USING SECTION

• keep out of eyes. Rinse with water to remove.

Stop use and ask doctor

OTC - STOP USE SECTION

• if rash occurs

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If swallowed, get medical help or contact a Poison Control Center right away.

Directions

DOSAGE & ADMINISTRATION SECTION

• Apply liberally 15 minutes before sun exposure. • children under 6 months: Ask a doctor • reapply at least every 2 hours • use a water resistant sunscreen if swimming or sweating. • Sun Protection Measures: Spending time in the sun increases your risk of skin cancer and early skin aging. To decrease this risk, regularly use sunscreen with a broad-spectrum SPF value of 15 or higher. • Limit time in the sun, especially from 10 a.m.– 2 p.m. • Wear long-sleeved shirts, pants, hats, and sunglasses.

Inactive ingredients

INACTIVE INGREDIENT SECTION

Water, Triheptanoin, Phenethyl Benzoate, Octyldodecyl Neopentanoate, C13-16 Isoalkane, Dimethicone, Phenoxyethanol, Glycereth-26, Hydroxyethyl Acrylate/Sodium Acryloyldimethyl Taurate Copolymer, Hydroxypropyl Starch Phosphate, Cetearyl Glucoside, Cetearyl Alcohol, Carbomer, Glycerin, Undecylenoyl Glycine, Capryloyl Glycine, Octyldodecanol, Sodium Hydroxide, Disodium EDTA, Sodium Hyaluronate, Sorbitan Isostearate, Polysorbate 60, Pyrus Malus (Apple) Fruit Extract, Tocopheryl Acetate, Haslea Ostrearia Extract, Palmaria Palmata Extract, Calendula Officinalis Flower Extract, Lavandula Angustifolia (Lavender) Oil, Pelargonium Graveolens Flower Oil, Linalool, Citronellol, Geraniol, Leuconostoc/Radish Root Ferment Filtrate, Rosmarinus Officinalis (Rosemary) Leaf Oil.

Other information

STORAGE AND HANDLING SECTION

• protect the product in this container from excessive heat and direct sun

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Jack Black

Authentic and Original

Double-Duty

Face Moisturizer

Broad Spectrum SPF 20 Sunscreen

with Blue Algae Extract

& Sea Parsley

SPF 20

labellabel

labellabel

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
124351b2-6dbf-42d0-9ea7-f0e299215f9aProduct name120210115

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
66738-771-12Jack Black Double Duty97 mL in 1 BOTTLELOTION972
66738-771-17Jack Black Double Duty251 mL in 1 BOTTLELOTION2512
66738-771-19Jack Black Double Duty473 mL in 1 BOTTLELOTION4732
66738-771-21Jack Black Double Duty44 mL in 1 TUBELOTION442

Products#

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

DailyMed product names page 1 of 1 · 37 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
66738-77166738-771-21, 66738-771-12, 66738-771-17, 66738-771-19

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 35 matching rows.

Name, UNII, Kind table
NameUNIIKind
PHENOXYETHANOLHIE492ZZ3TIACT
PYRUS MALUS (APPLE) FRUITB423VGH5S9IACT
HASLEA OSTREARIAY87200QHN9IACT
PALMARIA PALMATA7832HOY4ZQIACT
PELARGONIUM GRAVEOLENS FLOWER OIL3K0J1S7QGCIACT
LEUCONOSTOC/RADISH ROOT FERMENT FILTRATED2QHA03458IACT
OCTYLDODECYL NEOPENTANOATEX8725R883TIACT
POLYSORBATE 60CAL22UVI4MIACT
CETEARYL ALCOHOL2DMT128M1SIACT
UNDECYLENOYL GLYCINE4D20464K2JIACT
SODIUM HYDROXIDE55X04QC32IIACT
CARBOMER0A5MM307FCIACT
OCTOCRYLENE5A68WGF6WMACTIB
AVOBENZONEG63QQF2NOXACTIB
WATER059QF0KO0RIACT
HYDROXYETHYL ACRYLATE/SODIUM ACRYLOYLDIMETHYL TAURATE COPOLYMER (45000 MPA.S AT 1%)86FQE96TZ4IACT
C13-16 ISOPARAFFINLED42LZG6OIACT
GLYCERINPDC6A3C0OXIACT
CAPRYLOYL GLYCINE8TY5YO42NJIACT
EDETATE DISODIUM7FLD91C86KIACT
CALENDULA OFFICINALIS FLOWERP0M7O4Y7YDIACT
GERANIOLL837108USYIACT
ROSMARINUS OFFICINALIS (ROSEMARY) LEAF OIL8LGU7VM393IACT
CETEARYL GLUCOSIDE09FUA47KNAIACT
SORBITAN ISOSTEARATE01S2G2C1E4IACT
.ALPHA.-TOCOPHEROL ACETATE9E8X80D2L0IACT
LINALOOLD81QY6I88EIACT
TRIHEPTANOIN2P6O7CFW5KIACT
PHENETHYL BENZOATE0C143929GKIACT
OCTYLDODECANOL461N1O614YIACT
SODIUM HYALURONATEYSE9PPT4THIACT
LAVANDULA ANGUSTIFOLIA (LAVENDER) OILZBP1YXW0H8IACT
CITRONELLOLP01OUT964KIACT
DIMETHICONE92RU3N3Y1OIACT
GLYCERETH-26NNE56F2N14IACT

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 Black Double DutyAVOBENZONE OCTOCRYLENEJack Black L.L.C.36d81d6d-4f9b-692d-e063-6294a90ad5592025-08-27WarningsExact identifier
ndc (package): 66738-771-12
ndc (package): 66738-771-19
ndc (package): 66738-771-21
ndc (package): 66738-771-17
ndc (product): 66738-771
ndc11 (package): 66738077117
ndc11 (package): 66738077121
ndc11 (package): 66738077112
ndc11 (package): 66738077119
spl id: 3d5fdd97-4317-a962-e063-6294a90a1da8
spl set id: 36d81d6d-4f9b-692d-e063-6294a90ad559

Reported adverse events (FAERS/openFDA)#

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