Home › NDC Lookup › Ingredients › Zinc Oxide Titanium Dioxide › 69555-0035-05
EcoStick Sunscreen SPF 35 Zinc Oxide, Titanium Dioxide 6 g/100mL; 7 g/100mL Stick, 15 mL — NDC 69555-0035-05 package photo

EcoStick Sunscreen SPF 35 Zinc Oxide, Titanium Dioxide 6 g/100mL; 7 g/100mL Stick, 15 mL

by Stream2Sea, LLC · 15 mL in 1 TUBE (69555-035-05)
NDC 69555-0035-05
🏷️ FDA NDC (as labeled) 69555-035-05 billing pads the product segment with a zero
This package
Contains15 mL Pack sizes5 compare ↓
Also comes in: 15 ml 69555-0035-01 15 ml 69555-0035-02 15 ml 69555-0035-03 15 ml 69555-0035-04
OTC On market Non-controlled
🗂️ Data synced Aug 27, 2026 · sources: openFDA · FDA label (DailyMed) · FDA Orange & Purple Book · First Databank · CMS NADAC, ASP, Medicare & Medicaid · RxNorm
📋 All sources & update times →

This page is curated, coded, and maintained by

Compiled from public FDA, CMS, DailyMed, NADAC, and related drug data sources. Editorial policy

🆔 Identity & classification

FDA NDC (as labeled) 69555-035-05
Product NDC 69555-035
11-digit billing NDC 69555003505
UNII SOI2LOH54Z, 15FIX9V2JP
UPC 0851061008258, 0851061008241, 0851061008234, 0851061008265 +1 more
Application # M020
SPL Set ID eba17b7a-5e96-4462-9b71-44c2bc577dce
Established class (EPC) Copper Absorption Inhibitor
Physiologic effect Decreased Copper Ion Absorption
DEA schedule Non-controlled
Marketing category OTC MONOGRAPH DRUG
Marketing status On market
FDA listing status Listed (active directory)
Marketing start 2021-02-15
Route TOPICAL
Dosage form STICK
Substance ZINC OXIDE; TITANIUM DIOXIDE
Why two NDCs? The FDA registers this code as 69555-035-05 — a 5-3-2 layout, and that's what's printed on the package and shown on DailyMed. For insurance claims, every NDC is standardized to a uniform 11-digit 5-4-2 format by adding a zero to the product segment → 69555-0035-05. Same drug, same package — only the format differs.
Where does this data come from?
Identifiers from the FDA openFDA NDC Directory and Structured Product Labeling; RxCUI from RxNorm (NLM); GPI from Medi-Span; GCN / HIC / AHFS / legend from First Databank.

🏭 Manufacturer & labeler

LabelerStream2Sea, LLC
FDA applicationM020 (OTC MONOGRAPH DRUG)
Labeler code69555
First marketedFeb 2021
Product typeHuman Otc Drug
Portfolio14 products on file
The labeler markets the product; the application holder owns the FDA approval. They’re often the same company but can differ (e.g. a repackager or an authorized generic). A mailing address / phone appears here when the manufacturer includes it in the product’s FDA label (not all do).
Where does this data come from?
Labeler, application holder and registered establishment from the FDA openFDA NDC Directory and Drugs@FDA; address/contact from the product’s FDA label.

🩺 Clinical

🧪 What is this product?

EcoStick Sunscreen SPF 35 is a topical sunscreen product in stick form that contains two mineral UV filters: zinc oxide and titanium dioxide. Both ingredients are commonly used in sunscreens to reflect and scatter ultraviolet light away from the skin. This product is marketed as an over-the-counter monograph drug, meaning it follows the FDA's established safety and labeling rules for sunscreen products rather than undergoing individual review.

Supplement & herbal interactions

🌿 Drug–supplement interaction checker →
Where does this data come from?
Plain-language summary from MedlinePlus (U.S. National Library of Medicine); supplement & herbal interactions and nutrient depletion data from the Natural Medicines database; our full guide is HelloPharmacist editorial content.

💊 What it looks like

Color blue / pink
One label can cover several strengths, so colors may be combined — always confirm a loose pill against the dispensed prescription label or a pharmacist.
Where does this data come from?
Physical description (imprint, shape, color, scoring, coating) from this product’s FDA Structured Product Labeling (SPL), mirrored from DailyMed / openFDA.

🧪 Inactive Ingredients / Excipients

Inactive ingredients, also called excipients, are components of the drug product other than the active ingredient. They may include fillers, dyes, coatings, preservatives, flavors, or other formulation ingredients.

💡 Tap an ingredient (hover on desktop) to see what it is and why it’s used.

  • UNII H4N855PNZ1
    Alpha-tocopherol is a form of vitamin E, a fat-soluble antioxidant derived from natural or synthetic sources. In medicines, it prevents oils and fats from breaking down and becoming rancid, protecting the product's stability and shelf life.
  • UNII EJ9JK8J58D
    A brown seaweed extract used as a thickener and stabilizer in medicines. It helps create the right texture and prevents separation of liquid or semi-solid formulations.
  • UNII 9L3TIH1UUE
    Spirulina platensis is a blue-green algae used as a natural colorant and nutritional ingredient in supplements and some medications. It provides a blue-green color and may add protein and vitamins to the product.
  • UNII 0C9AC7D6XU
    A plant-derived fat from shea nut kernels that remains after soap-making. It acts as a moisturizer, emollient, and texture enhancer in topical formulations, helping soften skin and improve product spreadability.
  • UNII P0M7O4Y7YD
    A plant extract from calendula flowers, traditionally used in formulations. It typically serves as a botanical ingredient that may provide color, fragrance, or skin-conditioning properties to topical products.
  • UNII WL0328HX19
    A natural plant-based wax derived from candelilla shrub leaves. It acts as a coating agent, hardener, and texture modifier to control how quickly the medicine releases and to improve the tablet or capsule's appearance and stability.
  • UNII R12CBM0EIZ
    A natural wax derived from a Brazilian palm tree, used as a coating and polish on tablets and capsules. It creates a smooth, shiny finish that protects the medicine and improves appearance.
  • UNII D072FFP9GU
    Cetyl esters wax is a waxy substance made from natural or synthetic fatty acids. It's used as a binder, hardening agent, and coating material to give tablets and capsules their structure and texture.
  • UNII FGL3685T2X
    Chamomile is a plant extract used in medications as a flavoring agent and for its mild soothing properties in formulations. It helps improve taste and aroma of the medicine.
  • UNII 2968PHW8QP
    A weak organic acid derived from citrus fruits or made through fermentation. It works as a buffer to control pH, a preservative to extend shelf life, and a flavoring agent in medications.
  • UNII 512OYT1CRR
    Cocoa butter is a natural fat extracted from cocoa beans. It's used in medicines as a base for suppositories and as a lubricant to help pills dissolve smoothly.
  • UNII Q9L0O73W7L
    Coconut oil is a natural fat extracted from coconut fruit. It's used in medicines as a lubricant, emollient, or carrier to help dissolve or deliver active ingredients smoothly through the formulation.
  • UNII 1K09F3G675
    Ferric oxide red is an inorganic iron compound used as a colorant in medicines. It gives tablets, capsules, or other dosage forms a red or reddish tint for identification and appearance.
  • UNII TM2TZD4G4A
    A plant-derived oily substance used as an emulsifier and solubilizer in medicines. It helps blend water and oil-based ingredients together and improves how the body absorbs certain active drugs.
  • UNII W2ZU1RY8B0
    A plant extract from green tea leaves. It's used as an antioxidant ingredient to help preserve the medicine and maintain its stability during storage.
  • UNII SCJ765569P
    Holy basil leaf is a plant-derived ingredient used in some formulations as a flavoring agent or botanical additive. It may contribute taste and aroma to the medicine.
  • UNII UDR641JW8W
    A plant-derived oil from jojoba seeds that has been broken down into smaller components. It acts as an emollient and skin-conditioning agent to help soften and smooth the product's texture.
  • UNII 7CVR7L4A2D
    A starch-derived carbohydrate produced by breaking down corn, potato, or tapioca starch. It functions as a filler and binder to give the medicine bulk and texture, and sometimes as a mild sweetener or texture enhancer in powders and tablets.
  • UNII C9H2L21V7U
    A fat derived from coconut or palm oil containing shorter fatty acid chains. It serves as a solvent and carrier to help dissolve or suspend active ingredients, improving absorption and stability in liquid formulations.
  • UNII V8A1AW0880
    Mica is a naturally occurring mineral that's ground into fine powder. It's used in medicines as a colorant and anti-caking agent to improve appearance and prevent clumping in tablets or powders.
  • UNII MJ95C3OH47
    A plant extract from olive leaves used in formulations as an antioxidant and preservative. It helps protect the medicine from degradation and extend shelf life.
  • UNII YXH47AOU0F
    A synthetic fatty acid used as a thickener and stabilizer in medicines. It helps create the right texture and prevents separation of ingredients in liquid or semi-solid formulations.
  • UNII EM5RP35463
    A plant extract from radish root used as a natural flavoring agent and colorant in medicines. It adds taste and visual appeal to oral formulations like tablets and liquids.
  • UNII ETJ7Z6XBU4
    Silicon dioxide is a naturally occurring mineral used as a glidant and anti-caking agent. It helps powder ingredients flow smoothly and prevents clumping during manufacturing and storage.
  • UNII MDL271E3GR
    Sorbitan olivate is an emulsifier derived from sorbitol and olive oil. It helps blend water and oil ingredients together to maintain consistent texture and appearance throughout the medicine.
  • UNII 4DGK8B7I3S
    A starch extracted from rice grains. It acts as a filler to add bulk to the tablet or capsule and as a disintegrant to help the medicine break apart and release its active ingredient in your body.
  • UNII 3W1JG795YI
    Sunflower oil is a natural vegetable oil derived from sunflower seeds. It serves as a solvent, lubricant, and carrier in medicines, helping dissolve active ingredients and improve how the medication flows and absorbs in the body.
  • UNII B8WCK70T7I
    Trehalose is a natural sugar made from two glucose molecules linked together. It's used in medicines as a filler to add bulk, a sweetener for taste, and a stabilizer to help keep active ingredients effective during storage.

28 inactive ingredients listed in the exact product block matched to this NDC.

The official label also statesExtracts of Camellia Sinenis (Green Tea) Leaf*, Ocimum Tinuiflorum(Tulsi) Leaf*, Alaria Esculenta (Wakame Seaweed)*, and Olea Europa(Olive) Leaf in Cocos Nucifera (Coconut) Oil*, Caprylic CapricTriglycerides, Helianthus Annuus (Sunflower) Seed Oil*,TheobromaCacao (Cocoa) Seed Butter, Copernicia Prunifera (Carnauba) Wax,Candelilla Cera Wax, Sorbitan Olivate, Butyrospermum Parkii (Shea Butter) Fruit, Cetyl Esters, Polyhydroxystearic Acid, Rice Starch, GlycerylCaprylate, Silica, Mica, Mixed Tocopherols (Vitamin E). WILD BLUE Extracts of Camellia Sinenis (Green Tea) Leaf*, Ocimum Tinuiflorum (Tulsi) Leaf*, Alaria Esculenta (Wakame Seaweed)*, and Olea Europa(Olive) Leaf in Cocos Nucifera (Coconut) Oil*, Caprylic Capric Triglycerides, Helianthus Annuus (Sunflower) Seed Oil*, Theobroma Cacao (Cocoa) Seed Butter, Copernicia Prunifera (Carnauba) Wax,Candelilla Cera Wax, Sorbitan Olivate, Butyrospermum Parkii (Shea Butter) Fruit, Cetyl Esters, Polyhydroxystearic Acid, Rice Starch, Glyceryl Caprylate, Silica, Mica, Spirulina Platensis Extract (and) Trehalose, Mixed Tocopherols (Vitamin E). WILD PINK Extracts of Camellia Sinenis (Green Tea) Leaf*, Ocimum Tinuiflorum (Tulsi) Leaf*, Alaria Esculenta (Wakame Seaweed)*, and Olea Europa (Olive) Leaf in Cocos Nucifera (Coconut) Oil*, Caprylic Capric Triglycerides, Helianthus Annuus (Sunflower) Seed Oil*, Theobroma Cacao (Cocoa) Seed Butter, Copernicia Prunifera (Carnauba) Wax, Candelilla Cera Wax, Sorbitan Olivate, Butyrospermum Parkii (Shea Butter) Fruit, Cetyl Esters, Polyhydroxystearic Acid, Rice Starch, Rice Starch, Glyceryl Caprylate, Silica, Mica, Raphanus Sativus (Radish) Root Extract (and) Citric Acid (and) Maltodextrin, Mixed Tocopherols (Vitamin E). TINTED Extracts of Camellia Sinenis (Green Tea) Leaf*, Ocimum Tinuiflorum (Tulsi) Leaf*, Alaria Esculenta (Wakame Seaweed)*, and Olea Europa (Olive) Leaf in Cocos Nucifera (Coconut) Oil*, Caprylic Capric Triglycerides, Helianthus Annuus (Sunflower) Seed Oil*, Theobroma Cacao (Cocoa) Seed Butter, Copernicia Prunifera (Carnauba) Wax, Candelilla Cera Wax, Sorbitan Olivate, Butyrospermum Parkii (Shea Butter) Fruit, Cetyl Esters, Polyhydroxystearic Acid, Rice Starch, Glyceryl Caprylate, Silica, Mica, Mixed Tocopherols (Vitamin E), Iron Oxides (C.I.77492, C.I. 77491, C.I. 77499) and Jojoba Esters SUNSCREEN 4 KIDS Extracts of Chamomilla Recutita (Chamomile) Flower* (and) Calendula Officinalis* (and) Camellia Sinensis (Green Tea) Leaf* (and) Ocimum Tenuiflorum (Tulsi) in Cocos Nucifera (Coconut) Oil*, Caprylic Capric Triglycerides, Helianthus Annuus (Sunflower) Seed Oil*, Theobroma Cacao (Cocoa) Seed Butter, Copernicia Prunifera (Carnauba) Wax, Candelilla Cera Wax, Sorbitan Olivate, Butyrospermum Parkii (Shea Butter) Fruit, Cetyl Esters, Polyhydroxystearic Acid, Rice Starch, Glyceryl Caprylate, Silica, Mica, Mixed Tocopherols (Vitamin E).

Label-section wording can be broader than the structured product block and may mention additional formulation ingredients.

Where does this data come from?
Data sourced from official FDA Structured Product Labeling (SPL) via DailyMed — ingredient classCode="IACT" elements from the exact product block matched by this NDC. Label-section narrative from DailyMed / the openFDA label index is shown separately when available.

Inactive ingredient FAQ

Are inactive ingredients the same for every manufacturer?
No. Inactive ingredients can differ by manufacturer, dosage form, strength, and package / product version.
Why might an inactive ingredient be missing?
Some SPLs do not provide a complete structured inactive-ingredient list, and older or unusual labels may only include the information in narrative text.
Can inactive ingredients matter?
Yes. They can matter for allergies, intolerances, dyes, gluten / lactose concerns, preservatives, and formulation differences — but confirm with a pharmacist or the manufacturer when it’s clinically important.

💲 Pricing

A drug doesn't have one price. Each row is a different public payment system, and none is what you'd pay at the counter — that depends on your insurance. The ⓘ on each row explains what it measures.

Price systemPer eachPer package
Retail pharmacies payNADAC · weekly Not in the retail survey — common for institutional, discontinued, or low-volume packs.
Medicaid paysCMS SDUD · 12 mo No recent Medicaid claims on file for this NDC — rare and low-volume NDCs are suppressed in the public data.
Medicare drug plans payPart D · quarterly No Part D plan price is available for this NDC in our data.
ℹ️
No price is published for this exact package yet. CMS surveys NADAC per package size, so a different pack of the same drug often has one.
Try another pack size: 15 ml 15 ml 15 ml 15 ml
Where does this data come from?
NADAC (National Average Drug Acquisition Cost) is the CMS weekly pharmacy-acquisition-cost survey — what pharmacies pay. ASP (Average Sales Price) is the CMS Medicare Part B drug-payment file, published quarterly. Medicaid pays is computed by us from CMS State Drug Utilization Data (total reimbursed ÷ units, trailing 12 months) — gross of rebates and inclusive of dispensing fees, so it reflects what Medicaid paid, not an acquisition cost. Medicare drug plans pay is the median negotiated point-of-sale unit cost across plans listing this NDC in the CMS quarterly Prescription Drug Plan pricing files, before rebates. The VA pays is the federal contract price (FSS, and the statutory Big 4 ceiling where listed) from the VA National Acquisition Center pharmaceutical price file. All are free public government data; each measures a different payer, so the figures are not directly comparable.

🔁 Therapeutic equivalents

ProductLabelerPackNADAC/unitTEStatusPrice vs. this
EcoStick Sunscreen SPF 35 6 g/100mL; 7 g/100mLthis 69555-0035-05 Stream2Sea, 15 ml — — FDA listed —
About this product: other versions of the same ingredient, strength and form are listed above, least expensive first, with FDA equivalence ratings where available.
Where does this data come from?
Equivalents are other NDCs of the same ingredient, form and route from the openFDA NDC Directory, ranked least-expensive-first by NADAC. Therapeutic-equivalence (AB) ratings come from the FDA Orange Book; biologics use the FDA Purple Book for biosimilar & interchangeable status.

⏳ Availability & generic status

🏛️
2021
On the market since
Feb 2021
📍
2026
Currently FDA-listed
5 years listed
🔒
·
No generic listed yet
brand only
ℹ️No FDA-approved generic found

We did not find an FDA-approved generic match for this exact strength, form and route.

Where does this data come from?
Patents and exclusivity from the FDA Orange Book (small-molecule drugs), refreshed from public FDA data. Generic launch timing is an estimate, not a guarantee.

🔬 Reported adverse events (FAERS)

Read carefully: FAERS reports are voluntary and unverified. Counts are not incidence, do not establish causation, are subject to reporting bias, and cannot be used to compare one drug to another. Shown for signal context only. Reports for Zinc Oxide, Titanium Dioxide — the ingredient across all brands.

Top reported reactions

Chemical Burn1
Condition Aggravated1
Dehydration1
Erythema1
Erythema Of Eyelid1
Eyelid Irritation1
Eyelid Oedema1

Reporter sex

3 reports
Female · 100%
Where does this data come from?
Adverse-event reports from the FDA Adverse Event Reporting System (FAERS) via openFDA. FAERS reports are voluntary and unverified — counts are not incidence and don’t establish causation.

📦 Packaging — all sizes for this product

Package NDCDescription Marketing startStatus
69555-0035-01 15 mL in 1 TUBE (69555-035-01) 2021-02-15 Active
69555-0035-02 15 mL in 1 TUBE (69555-035-02) 2021-02-15 Active
69555-0035-03 15 mL in 1 TUBE (69555-035-03) 2021-02-15 Active
69555-0035-04 15 mL in 1 TUBE (69555-035-04) 2021-02-15 Active
69555-0035-05 You're viewing this 15 mL in 1 TUBE (69555-035-05) 2021-02-15 Active

Pack size FAQ

What quantity is in NDC 69555-0035-05?
NDC 69555-0035-05 contains 15 mL — 15 ml in 1 tube.
What is the difference between NDC 69555-0035-05 and NDC 69555-0035-01?
Both are EcoStick Sunscreen SPF 35 Zinc Oxide, Titanium Dioxide 6 g/100mL; 7 g/100mL Stick — the drug itself is identical. NDC 69555-0035-05 is the 15 mL package, while NDC 69555-0035-01 is the 15 ml package.
What NDC number is used to bill for this package of EcoStick Sunscreen SPF 35 Zinc Oxide, Titanium Dioxide 6 g/100mL; 7 g/100mL Stick?
Bill NDC 69555-0035-05 — the 11-digit billing format is 69555003505. Pharmacy and medical claims use the 11-digit form; the FDA label may print a shorter form of the same code.

🧭 About this NDC listing & data coverage

Over-the-counter (OTC) product
What data is (and isn’t) available for this NDC — tap to expand
NDC identity (package / product / labeler codes) ✓ Available
Labeler ✓ Available
Product & package description ✓ Available
Marketing category & status ✓ Available
Active ingredient / dosage form / route ✓ Available
FDA label (SPL via DailyMed) ✓ Available
Package photos ✓ Available
Inactive ingredients (structured) ✓ Available
NADAC pharmacy acquisition price (CMS) — Not published for this NDC CMS publishes NADAC only for NDCs reported in its retail-pharmacy survey.
Orange Book / therapeutic-equivalence data — Not published for this NDC Applies only to products approved under an NDA/ANDA; many listings are out of scope.
HCPCS J-code billing crosswalk — Not published for this NDC Most self-administered / retail products have no J-code — that is normal.
Medicaid utilization (CMS SDUD) — Not published for this NDC CMS reports utilization only for NDCs with Medicaid claims above its privacy threshold.
“Not published” reflects what the public FDA / CMS / NLM sources provide for this exact package code — it is a property of the data feeds, not a judgment about the product.

Questions about this listing

Is this NDC FDA-approved?
An NDC listing does not by itself establish FDA approval — the NDC Directory records that a product is listed with FDA, not that it was reviewed and approved. This listing's marketing category is "Otc Monograph Drug". Products approved under an application carry an NDA, ANDA, or BLA number.
Why is there no price listed?
The pricing shown on our NDC pages comes from CMS NADAC, a voluntary survey of retail community pharmacy invoices. CMS does not publish a NADAC for every NDC — packages outside the retail survey (institutional and hospital products, bulk packages, discontinued items, and many OTC items) may never receive one. A missing price reflects the survey's scope, not this product's actual cost, and does not mean the product is free or unavailable.
Is the NDC printed on the package the same as the 11-digit billing NDC?
Yes, they identify this exact package in different formats. The FDA registers it as 69555-035-05, which is what is printed on the packaging and shown on DailyMed. Insurance claims use a fixed 11-digit 5-4-2 format, so the short segment is padded with a leading zero: 69555-0035-05, written without dashes as 69555003505. The Identity section at the top of this page lists every form of this code.
What do the three segments of this NDC mean?
In 69555-0035-05, the first segment (69555) is the labeler code FDA assigned to Stream2Sea, LLC; the middle segment (0035) identifies this specific product — its ingredient, strength, and dosage form; and the last segment (05) identifies this exact package size and type. Together they name one specific package of one specific product.
Is this package still being marketed?
Yes, per the latest FDA NDC Directory data on this page: this package is listed as actively marketed, with no marketing end date reported by Stream2Sea, LLC. Listing status can change — the directory data on this page refreshes weekly.
Does this product come in other package sizes?
Yes — the FDA directory lists 4 other package presentations of this same product, including 15 ml (69555-0035-01), 15 ml (69555-0035-02), 15 ml (69555-0035-03). Each has its own NDC and its own page — see the package list near the top of this page.
Who lists this product with the FDA?
Stream2Sea, LLC is the labeler of record for this NDC — the company under whose FDA-assigned code the package is listed. The labeler may be the manufacturer itself or a distributor marketing the product under its own code.
Do I need a prescription for this product?
This NDC is listed with FDA as an over-the-counter product, so it does not require a prescription. Follow the package directions, and ask your pharmacist if you are unsure whether it is right for you.
This page identifies an FDA-listed package (the NDC) and reports public regulatory and pricing data about the listing. It is reference information, not a medical recommendation — talk to your pharmacist or prescriber about your own medication.
Where does this data come from?
Listing facts (marketing category, packager status, marketing dates) from the FDA openFDA NDC Directory; label availability from DailyMed; pricing coverage from CMS NADAC; equivalence scope from the FDA Orange Book.

📄 FDA label — Drug Facts FDA SPL

The complete FDA label for this product — the official Drug Facts labeling, verbatim, section by section. Jump with a chip, search within the label, or expand everything.
🎯 Indications and Usage ⏱️ Dosage and Administration ⚠️ Warnings 📦 Storage and Handling 🧪 Active Ingredient 🧪 Inactive Ingredients 🎯 Purpose
🎯 Indications and Usage 28 words ▾

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

⏱️ Dosage and Administration 96 words ▾

Directions Apply liberally on cleansed skin prior to sun exposure. Reapply: after 80 minutes of swimming or sweating / immediately after towel drying / at least every 2 hours 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 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: Ask a doctor.

⚠️ Warnings 38 words ▾

Warnings ​ 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.

📦 Storage and Handling 11 words ▾

Other information Protect this product from excessive heat and direct sun.

🧪 Active Ingredient 10 words ▾

Active Ingredients Titanium Dioxide (Non-Nano) 7% Zinc Oxide (Non-Nano) 6%

🧪 Inactive Ingredients ~2 min read ▾

Inactive ingredients Extracts of Camellia Sinenis (Green Tea) Leaf*, Ocimum Tinuiflorum(Tulsi) Leaf*, Alaria Esculenta (Wakame Seaweed)*, and Olea Europa(Olive) Leaf in Cocos Nucifera (Coconut) Oil*, Caprylic CapricTriglycerides, Helianthus Annuus (Sunflower) Seed Oil*,TheobromaCacao (Cocoa) Seed Butter, Copernicia Prunifera (Carnauba) Wax,Candelilla Cera Wax, Sorbitan Olivate, Butyrospermum Parkii (Shea Butter) Fruit, Cetyl Esters, Polyhydroxystearic Acid, Rice Starch, GlycerylCaprylate, Silica, Mica, Mixed Tocopherols (Vitamin E).

WILD BLUE Extracts of Camellia Sinenis (Green Tea) Leaf*, Ocimum Tinuiflorum (Tulsi) Leaf*, Alaria Esculenta (Wakame Seaweed)*, and Olea Europa(Olive) Leaf in Cocos Nucifera (Coconut) Oil*, Caprylic Capric Triglycerides, Helianthus Annuus (Sunflower) Seed Oil*, Theobroma Cacao (Cocoa) Seed Butter, Copernicia Prunifera (Carnauba) Wax,Candelilla Cera Wax, Sorbitan Olivate, Butyrospermum Parkii (Shea Butter) Fruit, Cetyl Esters, Polyhydroxystearic Acid, Rice Starch, Glyceryl Caprylate, Silica, Mica, Spirulina Platensis Extract (and) Trehalose, Mixed Tocopherols (Vitamin E).

WILD PINK Extracts of Camellia Sinenis (Green Tea) Leaf*, Ocimum Tinuiflorum (Tulsi) Leaf*, Alaria Esculenta (Wakame Seaweed)*, and Olea Europa (Olive) Leaf in Cocos Nucifera (Coconut) Oil*, Caprylic Capric Triglycerides, Helianthus Annuus (Sunflower) Seed Oil*, Theobroma Cacao (Cocoa) Seed Butter, Copernicia Prunifera (Carnauba) Wax, Candelilla Cera Wax, Sorbitan Olivate, Butyrospermum Parkii (Shea Butter) Fruit, Cetyl Esters, Polyhydroxystearic Acid, Rice Starch, Rice Starch, Glyceryl Caprylate, Silica, Mica, Raphanus Sativus (Radish) Root Extract (and) Citric Acid (and) Maltodextrin, Mixed Tocopherols (Vitamin E).

TINTED Extracts of Camellia Sinenis (Green Tea) Leaf*, Ocimum Tinuiflorum (Tulsi) Leaf*, Alaria Esculenta (Wakame Seaweed)*, and Olea Europa (Olive) Leaf in Cocos Nucifera (Coconut) Oil*, Caprylic Capric Triglycerides, Helianthus Annuus (Sunflower) Seed Oil*, Theobroma Cacao (Cocoa) Seed Butter, Copernicia Prunifera (Carnauba) Wax, Candelilla Cera Wax, Sorbitan Olivate, Butyrospermum Parkii (Shea Butter) Fruit, Cetyl Esters, Polyhydroxystearic Acid, Rice Starch, Glyceryl Caprylate, Silica, Mica, Mixed Tocopherols (Vitamin E), Iron Oxides (C.I.77492, C.I.

77491, C.I. 77499) and Jojoba Esters SUNSCREEN 4 KIDS Extracts of Chamomilla Recutita (Chamomile) Flower* (and) Calendula Officinalis* (and) Camellia Sinensis (Green Tea) Leaf* (and) Ocimum Tenuiflorum (Tulsi) in Cocos Nucifera (Coconut) Oil*, Caprylic Capric Triglycerides, Helianthus Annuus (Sunflower) Seed Oil*, Theobroma Cacao (Cocoa) Seed Butter, Copernicia Prunifera (Carnauba) Wax, Candelilla Cera Wax, Sorbitan Olivate, Butyrospermum Parkii (Shea Butter) Fruit, Cetyl Esters, Polyhydroxystearic Acid, Rice Starch, Glyceryl Caprylate, Silica, Mica, Mixed Tocopherols (Vitamin E).

🎯 Purpose 2 words ▾

Purpose Sunscreen

Source: FDA Structured Product Labeling, mirrored from DailyMed / openFDA. Prefer the government’s original formatting? View this label on DailyMed ↗
← 69555-0032-02 · Stream2Sea 69555-0036-04 · Stream2Sea, →
For educational and professional reference only — not medical advice. Pricing reflects published NADAC and CMS ASP (free public data) and may differ from your acquisition cost; always verify before billing or dispensing.