OCTOCRYLENE, ZINC OXIDE, TITANIUM DIOXIDE, OCTINOXATE

Manufacturer
SIBORG
Effective date
2018-10-12
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
legacy-cache
Hydrated at
2026-08-02 00:49:04

Label at a glance#

ProductSirot Hand and Body Trio Transformative Glass Technology Complete Age Resistance Day and Night
Active ingredientOCTINOXATE, OCTOCRYLENE, TITANIUM DIOXIDE, ZINC OXIDE
Label structure7 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

apply liberally and evenly 15 minutes before sun exposure Reapply at least every 2 hours Use a water resistant sunscreen if swimming or sweating Sun Protection Measures: Spending tim 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, e...

Label contents#

Full prescribing information#

Active ingredients

OTC - ACTIVE INGREDIENT SECTION

Octinoxate 6.0%
Octocrylene 2.5%
Titanium dioxide 0.22%
Zinc oxide 2.9%

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 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 a doctor if

OTC - STOP USE SECTION

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 and evenly 15 minutes before sun exposure
  • Reapply at least every 2 hours
  • Use a water resistant sunscreen if swimming or sweating
  • Sun Protection Measures: Spending tim 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
  • Children under 6 months of age: Ask a doctor

Inactive ingredients

INACTIVE INGREDIENT SECTION

water (aqua), glycerin, cetearyl alcohol, octyldodecanol, isononyl isononanoate, butylene glycol, dimethicone, aluminum starch octenylsuccinate, cetearyl olivate, cetyl alcohol, sorbitan olivate, panthenol, sodium silicate, dioleyl tocopheryl methylsilanol, macadamia ternifolia seed oil, shea (butyrospermum parkii) butter, aloe (aloe barbadensis) leaf extract, sodium ascorbyl phosphate, tea (camellia sinensis) leaf extract, ylang ylang (cananga odorata) flower oil, tribehenin, ceramide ng, peg-10 phytosterol, niacinamide, oleyl alcohol, sodium hyaluronate crosspolymer,hydrogenated ethylhexyl olivate, xanthan gum, polysorbate 60, caprylyl glycol, mica, citric acid, acrylates/c10-30 alkyl acrylate crosspolymer, hexylene glycol, triethoxycaprylylsilane, tocopheryl acetate, disodium edta, hydrogenated olive oil unsaponifiables, c12-15 alkyl benzoate, pentylene glycol, hydrogenated lecithin, ethylhexylglycerin, palmitoyl hexapeptide-12, retinyl palmitate, sodium methyl stearoyl taurate, fragrance (*100% natural fragrance), phenoxyethanol

Package Labeling:

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Label2Label2LABELLABEL

Package Labeling:

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Outer PackageOuter PackageInner PackageInner Package

Products#

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NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
70803-45170803-451-01
70803-42070803-420-00

Ingredients#

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

DailyMed ingredient rows page 1 of 2 · 44 matching rows.

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
9a2a81f1-bd4e-4d25-e053-2995a90a85556ccb45b2-67be-f1eb-e053-2a91aa0a2de12019-12-20WarningsExact identifier
spl set id: 6ccb45b2-67be-f1eb-e053-2a91aa0a2de1

Reported adverse events (FAERS/openFDA)#

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