TATCHA The Milky Sunscreen - TATCHA INC.

Manufacturer
TATCHA INC.
Effective date
2026-10-01
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
daily-update
Hydrated at
2026-10-06 02:03:30

Label at a glance#

ProductTATCHA The Milky Sunscreen
Active ingredientAVOBENZONE, HOMOSALATE, OCTISALATE
Label structure9 sections

Indications and uses

• Helps prevent sunburn. • If used as directed with other sun protection measures (see Directions ), decreases the risk of skin cancer and early skin aging caused by the sun.

Dosage and administration

Shake lightly before use. Apply liberally 15 minutes before sun exposure. Reapply at least every 2 hours. Use a water-resistant sunscreen if swimming or sweating. 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, regularly use a sunscreen with a Broad Spectrum SPF value of 15 or higher and other s...

Label contents#

Full prescribing information#

Active Ingredients

OTC - ACTIVE INGREDIENT SECTION

Avobenzone 2.3%
Homosalate 6.6%
Octisalate 4.5%

Purpose

OTC - PURPOSE SECTION

Sunscreen

Uses

INDICATIONS & USAGE SECTION

• Helps prevent sunburn.
• If used as directed with other sun protection measures (see Directions), decreases the risk of skin cancer and early skin aging caused by the sun.

Warnings

WARNINGS SECTION

For external use only.

  • Do not useon damaged or broken skin.
  • When using this productkeep out of eyes. Rinse with water to remove.
  • Stop use and ask a doctorif a rash occurs.
  • Keep out of reach of children. If the product is swallowed, get medical help or contact a Poison Control Center right away

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Directions

DOSAGE & ADMINISTRATION SECTION

  • Shake lightly before use.
  • Apply liberally 15 minutes before sun exposure.
  • Reapply at least every 2 hours.
  • Use a water-resistant sunscreen if swimming or sweating.
  • 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, regularly use a sunscreen with a Broad Spectrum SPF value of 15 or higher and other sun protection measures including: Limit time in the sun, especially from 10 a.m.–2 p.m.
  • Wear long-sleeved shirts, pants, hats, and sunglasses

Other Information

SPL UNCLASSIFIED SECTION

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

Inactive Ingredients

INACTIVE INGREDIENT SECTION

WATER, SACCHAROMYCES/RICE FERMENT FILTRATE, BUTYLENE GLYCOL, PENTYLENE GLYCOL, POLYGLYCERYL-10 LAURATE, PROPANEDIOL, CAMELLIA SINENSIS LEAF EXTRACT, CLADOSIPHON OKAMURANUS EXTRACT, ALOE BARBADENSIS LEAF EXTRACT, ACRYLATES/C10-30 ALKYL ACRYLATE CROSSPOLYMER, CAPRYLIC/CAPRIC TRIGLYCERIDE, HYDROGENATED PHOSPHATIDYLCHOLINE, TOCOPHEROL, ECTOIN, CAPRYLYL GLYCOL, TOCOPHERYL ACETATE, FRAGRANCE, ETHYLHEXYLGLYCERIN, SODIUM HYDROXIDE, SILICA, PHENOXYETHANOL, IRON OXIDES (CI 77491)

Questions?

SPL UNCLASSIFIED SECTION

Call toll-free (877) 322-8633

Product Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

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Products#

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NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
69417-16369417-163-01, 69417-163-02, 69417-163-03, 69417-163-04

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 22 matching rows.

Source Document#

Source XML

Older Hydrated Versions#

Version, Effective date, Source table
VersionEffective dateSourceHydrated
12026-02-27full-release2026-06-01 01:48:46

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
TATCHA The Milky SunscreenAVOBENZONE, HOMOSALATE ,OCTISALATETATCHA INC.43f2ede2-21bf-4f4d-a2b0-83e166868b2d2026-02-27WarningsExact identifier
ndc (package): 69417-163-01
ndc (package): 69417-163-02
ndc (product): 69417-163
ndc11 (package): 69417016301
ndc11 (package): 69417016302
spl set id: 43f2ede2-21bf-4f4d-a2b0-83e166868b2d

Reported adverse events (FAERS/openFDA)#

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