FDA.reportPublic FDA data

Jack Black Double-Duty Face Moisturizer

Manufacturer
Jack Black, LLC
Effective date
2026-09-08
Label type
HUMAN OTC DRUG LABEL
Version
9
Source
daily-update
Hydrated at
2026-09-11 03:02:54

Label at a glance#

ProductDouble-Duty Face Moisturizer
Active ingredientAVOBENZONE, OCTINOXATE
Label structure10 sections

Dosage and administration

Apply liberally 15 minutes before sun exposure Use a water resisitant sunscreen if swimming or sweating Reapply at least every two hours Children under 6 months: ask a doctor. Sun Protection Measures:    Spending time in the sun increases your risk of skin cancer and early skin aging.  To decrease this risk, use sunscreen with a broad spectrum SPF15 or higher    Limit time in the sun, especxially from 10 a.m. - 2 ...

Label contents#

Full prescribing information#

Active Ingredients

OTC - ACTIVE INGREDIENT SECTION

Avobenzone   2.2%   Sunscreen

Octinoxate     7.5%   Sunscreen

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Purified Water, Cyclopentasiloxane, Octyldodecyl Neopentanoate, Phenylethyl Benzoate, Dimethicone, Glycereth-26, Hydroxyethyl Acrylate / Sodium Acryloyl Dimethyl Taurate Copolymer, Phenoxyethanol, Hydroxypropyl Starch Phosphate, Cetearyl Glucoside, Carbomer, Pyrus Malus (Apple) Fruit Extract, Butylene Glycol, Sodium Hydroxide, Disodium EDTA, Sodium Hyaluronate, Lavendula Angustifolia (Lavender) Oil, Iodopropynyl Butylcarbamate, Pelargonium Graveolens (Geranium) Flower Oil, Rosmarinus Officinalis (Rosemary) Leaf Oil, Lecithin, Melissa Officinalis (Balm Mint) Extract, Haslea Ostreaia (Blue Algae) Extract, Palmaria Palmata (Sea Parsley) Extract, Calendula Officinalis (Calendula) Flower Extract, Glycerin, Leontopodium Alöinum (Edelweiss) Extract, Artemisia Umbelliformis Extract, Buddleja Davidii Leaf Extract, Peucedanum Ostruthium Leaf Extract, Tocopheryl Acetate, Retinyl Palmitate, Anthemis Nobilis (Roman Chamomile) Flower Oil

Use

INDICATIONS & USAGE SECTION

Helps prevent sunburn

Use

OTC - PURPOSE SECTION

Helps prevent sunburn

Warnings

WARNINGS SECTION

  • For external use only
  • Do not use on damaged or broken skin
  • Stop use and ask doctor if rash occurs
  • When using this product keep out of eyes.  Rinse with water to remove
  • Keep out of reach of children
  • If swallowed, get medical help or contact Poison Control Center right away

Directions

DOSAGE & ADMINISTRATION SECTION

  • Apply liberally 15 minutes before sun exposure
  • Use a water resisitant sunscreen if swimming or sweating
  • Reapply at least every two hours
  • Children under 6 months: ask a doctor.
  • Sun Protection Measures:
  •    Spending time in the sun increases your risk of skin cancer and early skin aging.  To decrease this risk, use sunscreen with a broad spectrum SPF15 or higher
  •    Limit time in the sun, especxially from 10 a.m. - 2 p.m.
  •    Wear long sleeve shirts, pants, hats and sunglasses.

KEEP OUT OF REACH OF CHILDREN

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

KEEP OUT OF REACH OF CHILDREN

Other Information

OTHER SAFETY INFORMATION

Protect product from excessive heat and driect sunlight.  You may report a serious adverse reaction from using this product to Jack Black at 1-877-766-3388.

Labeling

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Jack Black Double-Duty Face MoisturizerJack Black Double-Duty Face Moisturizer

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
66738-02066738-020-03, 66738-020-04, 66738-020-19, 66738-020-01, 66738-020-16, 66738-020-50, 66738-020-02

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
AVOBENZONEG63QQF2NOXACTIB
OCTINOXATE4Y5P7MUD51ACTIB
WATER059QF0KO0RIACT
CYCLOMETHICONENMQ347994ZIACT
OCTYLDODECYL NEOPENTANOATEX8725R883TIACT
PHENETHYL BENZOATE0C143929GKIACT
HASLEA OSTREARIAY87200QHN9IACT
HYALURONATE SODIUMYSE9PPT4THIACT
LECITHIN, SOYBEAN1DI56QDM62IACT
GLYCERINPDC6A3C0OXIACT
LAVENDER OILZBP1YXW0H8IACT
ROSEMARY OIL8LGU7VM393IACT
MELISSA OFFICINALIS LEAF OILPTP6R7263MIACT
PEUCEDANUM OSTRUTHIUM LEAF86P27YRR6YIACT
BUDDLEJA DAVIDII LEAFX380815D32IACT
PELARGONIUM GRAVEOLENS FLOWER OIL3K0J1S7QGCIACT
DIMETHICONE92RU3N3Y1OIACT
GLYCERETH-26NNE56F2N14IACT
HYDROXYETHYL ACRYLATE/SODIUM ACRYLOYLDIMETHYL TAURATE COPOLYMER (100000 MPA.S AT 1.5%)86FQE96TZ4IACT
PHENOXYETHANOLHIE492ZZ3TIACT
CETEARYL GLUCOSIDE09FUA47KNAIACT
CARBOMER 934Z135WT9208IACT
BUTYLENE GLYCOL3XUS85K0RAIACT
SODIUM HYDROXIDE55X04QC32IIACT
EDETATE DISODIUM7FLD91C86KIACT
IODOPROPYNYL BUTYLCARBAMATE603P14DHEBIACT
DULSE7832HOY4ZQIACT
.ALPHA.-TOCOPHEROL ACETATE9E8X80D2L0IACT
VITAMIN A PALMITATE1D1K0N0VVCIACT
CALENDULA OFFICINALIS FLOWERP0M7O4Y7YDIACT
LEONTOPODIUM NIVALE SUBSP. ALPINUM FLOWERMWN6IZU3XMIACT
APPLE FRUIT OIL9NT987I3A8IACT
ARTEMISIA UMBELLIFORMIS FLOWER91OLL9AJ7DIACT
CHAMAEMELUM NOBILE FLOWER OILUB27587839IACT
CARBOMER HOMOPOLYMER TYPE A (ALLYL PENTAERYTHRITOL CROSSLINKED)F68VH75CJCIACT

Source Document#

Source XML

Older Hydrated Versions#

Version, Effective date, Source table
VersionEffective dateSourceHydrated
82023-11-07full-release2026-05-31 23:59:33

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
Double-Duty Face MoisturizerMOSITURIZING SUNSCREENJack Black, LLC672be406-e3a1-47b4-8ef6-ee2b62baae962026-09-08WarningsExact identifier
ndc (package): 66738-020-02
ndc (package): 66738-020-19
ndc (package): 66738-020-03
ndc (package): 66738-020-04
ndc (package): 66738-020-50
ndc (package): 66738-020-01
ndc (package): 66738-020-16
ndc (product): 66738-020
ndc11 (package): 66738002001
ndc11 (package): 66738002003
ndc11 (package): 66738002050
ndc11 (package): 66738002019
ndc11 (package): 66738002004
ndc11 (package): 66738002002
ndc11 (package): 66738002016
spl id: 5aff192a-cd63-e163-e063-6294a90ab621
spl set id: 672be406-e3a1-47b4-8ef6-ee2b62baae96

Reported adverse events (FAERS/openFDA)#

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