TheFaceShop Jelly Pact

Manufacturer
THEFACESHOP CO., LTD. | THEFACESHOP NORTH AMERICA, INC.
Effective date
2014-11-20
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 22:41:37

Label at a glance#

ProductTheFaceShop Jelly Pact 34200187
Active ingredientOCTINOXATE, TITANIUM DIOXIDE, ZINC OXIDE
Label structure9 sections

Dosage and administration

Apply generously and evenly 15 minutes before sun exposure. Children under 6 months of age: Ask a doctor. Apply to all skin exposed to the sun. Skin Cancer/Skin Aging Alert: Spending time in the sun increases your risk of skin cancer and early skin aging. This product has been shown only to help prevent sunburn, not skin cancer or early skin aging. Reapply at least every 2 hours. Use a water-resistant sunscreen if...

Label contents#

Full prescribing information#

Active Ingredients

OTC - ACTIVE INGREDIENT SECTION

Octinoxate 6.0 %, Titanium Dioxide 17.1, Zinc Oxide 2.9 % %,

Purpose

OTC - PURPOSE SECTION

Sunscreen

Sunscreen

Sunscreen

Warnings

WARNINGS SECTION

For external use only.

Do not use on damaged or broken skin

When using this product keep out of eyes. Rinse with water to remove.

Stop use and ask a doctor if rash occurs.

Keep out of reach of children. If product is swallowed, get medical help or contact a Poison Control Center right away.

Close the cover to prevent the moisturizing ingredients from evaporating.

Directions

OTC - WHEN USING SECTION

  • Apply generously and evenly 15 minutes before sun exposure.
  • Children under 6 months of age: Ask a doctor.
  • Apply to all skin exposed to the sun.
  • Skin Cancer/Skin Aging Alert: Spending time in the sun increases your risk of skin cancer and early skin aging. This product has been shown only to help prevent sunburn, not skin cancer or early skin aging.
  • Reapply at least every 2 hours.
  • Use a water-resistant sunscreen if swimming or sweating.
  • Apply an adequate amount on face in a light patting motion by using puff.

Other Information

OTHER SAFETY INFORMATION

Protect the product in this container from excessive heat and direct sun

May stain or damage some fabrics or surfaces

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Mica (CI 77019), Caprylic/Capric Triglyceride, Polymethyl Methacrylate, Dimethicone, Talc, Methyl Methacrylate Crosspolymer, Diisostearyl Malate, Dimethicone/Vinyl Dimethicone Crosspolymer, Pentylene Glycol, Methicone, Lauroyl Lysine, Aluminum Hydroxide, , Silica, , Glycyrrhiza Glabra (Licorice) Root Extract, , Hydroxyapatite, Argania Spinosa Kernel Oil, Persea Gratissima (Avocado) Oil, Olea Europaea (Olive) Fruit Oil, Lilium Candidum Bulb Extract, Fragrance(Parfum), Iron Oxides (CI 77491, CI 77492, CI 77499)

OTC - QUESTIONS SECTION

Questions or comments? Call 1-866-638-8417

Distributed by:

SPL UNCLASSIFIED SECTION

THEFACESHOP NORTH AMERICA, INC.

Santa Fe Springs, CA 90670

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

JELLY PACT

SUNSCREEN GEL SPF50

01 RADIANT BEIGE

LabelLabel

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
51523-187-362020-01-31C16284748780-19d75b9d0-ddb0-f424-e053-dadaa90a57ceTheFaceShop Jelly Pact 34200187

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
51523-187-36TheFaceShop Jelly Pact342001871 in 1 CARTONGEL11
51523-187-36TheFaceShop Jelly Pact3420018710 g in 1 CONTAINERGEL101

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
51523-187THEFACESHOP JELLY PACT 34200187 (OCTINOXATE, TITANIUM OXIDE AND ZINC OXIDE GEL) GEL [THEFACESHOP CO., LTD.]1Legacy NDC, 2 package rows20150205_0822fdb2-c660-12ec-e054-00144ff8d46c.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
OCTINOXATEACTIVE INGREDIENT4Y5P7MUD511
TITANIUM DIOXIDEACTIVE INGREDIENT15FIX9V2JP1
ZINC OXIDEACTIVE INGREDIENTSOI2LOH54Z1
OCTINOXATEACTIVE MOIETY4Y5P7MUD511
TITANIUM DIOXIDEACTIVE MOIETY15FIX9V2JP1
ZINC OXIDEACTIVE MOIETYSOI2LOH54Z1
MICAINACTIVE INGREDIENTV8A1AW08801

Products#

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

DailyMed product names page 1 of 1 · 6 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
51523-18751523-187-36

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 4 matching rows.

Source Document#

Source XML · Source PDF

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
0822fdb2-c661-12ec-e054-00144ff8d46c0822fdb2-c660-12ec-e054-00144ff8d46c2014-11-20WarningsExact identifier
spl id: 0822fdb2-c661-12ec-e054-00144ff8d46c
spl set id: 0822fdb2-c660-12ec-e054-00144ff8d46c

Reported adverse events (FAERS/openFDA)#

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