Home › NDC Lookup › Ingredients › Octocrylene, Homosalate, Octisalate, Avo... › 76147-0400-45
StriVectin TL Advanced Tightening Neck and Chest Broad Spectrum SPF 35 Sunscreen Octocrylene, Homosalate, Octisalate, Avobenzone 3 g/100mL; 10 g/100mL; 7 g/100mL; 4.5 g/100mL Cream — NDC 76147-0400-45 package photo

StriVectin TL Advanced Tightening Neck and Chest Broad Spectrum SPF 35 Sunscreen Octocrylene, Homosalate, Octisalate, Avobenzone 3 g/100mL; 10 g/100mL; 7 g/100mL; 4.5 g/100mL Cream

by StriVectin Operating Company, Inc. · 1 BOTTLE, PUMP in 1 CARTON (76147-400-45) / 45 mL in 1 BOTTLE, PUMP
NDC 76147-0400-45
🏷️ FDA NDC (as labeled) 76147-400-45 billing pads the product segment with a zero
This package
Contains45 mL in 1 bottle, pump Pack sizes2 compare ↓
Also comes in: 10 mL 76147-0400-10
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) 76147-400-45
Product NDC 76147-400
11-digit billing NDC 76147040045
UNII G63QQF2NOX, 5A68WGF6WM, V06SV4M95S, 4X49Y0596W
Application # M020
SPL Set ID 4873a262-a19b-555e-e063-6394a90a182a
DEA schedule Non-controlled
Marketing category OTC MONOGRAPH DRUG
Marketing status On market
FDA listing status Listed (active directory)
Marketing start 2026-01-15
Route TOPICAL
Dosage form CREAM
Substance AVOBENZONE; OCTOCRYLENE; HOMOSALATE; OCTISALATE
Why two NDCs? The FDA registers this code as 76147-400-45 — 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 → 76147-0400-45. 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

LabelerStriVectin Operating Company, Inc.
FDA applicationM020 (OTC MONOGRAPH DRUG)
Labeler code76147
First marketedJan 2026
Product typeHuman Otc Drug
Portfolio5 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?

StriVectin TL Advanced Tightening Neck and Chest is a topical cream formulated as an over-the-counter sunscreen product marketed under the FDA's OTC monograph rules. It contains four active sunscreen ingredients (avobenzone, homosalate, octisalate, and octocrylene) that are typically used to absorb and filter ultraviolet (UV) radiation from the sun. This product is designed to be applied to the skin of the neck and chest area to provide broad-spectrum sun protection. The cream base also contains other ingredients intended to provide moisturizing and skin-tightening benefits.

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.

🧪 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 TR046Y3K1G
    A liquid alcohol derived from petroleum or plant sources. It acts as a solvent and humectant in medicines, helping dissolve active ingredients and retain moisture in the formulation.
  • UNII 8Z5ZAL5H3V
    A synthetic polymer made from acrylate compounds. It acts as a thickener and stabilizer in topical formulations, helping create the right texture and prevent separation of ingredients.
  • UNII 3K9958V90M
    A liquid solvent derived from fermentation or chemical synthesis. In medicines, alcohol dissolves active ingredients, helps preserve the product, and improves how the body absorbs certain drugs.
  • UNII TRW2FUF47H
    A plant-derived powder from marshmallow root used as a binder and thickener in medicines. It helps hold ingredients together and can soothe irritated surfaces in throat lozenges and syrups.
  • UNII 0O72R8RF8A
    A group of organic compounds that form proteins. Amino acids in medicines typically serve as buffers to maintain pH balance, or as stabilizers and bulking agents to help preserve the active ingredient and improve the product's stability.
  • UNII LU49E6626Q
    A synthetic organic compound used as a pH buffer and neutralizing agent in medicines. It helps maintain the proper acidity level in liquid formulations to improve stability and comfort.
  • UNII N4G8379626
    A plant-based oil extracted from rapeseed (also called canola). It's used in medicines as an emulsifier and lubricant to help blend ingredients together and improve how the product flows and feels.
  • UNII K67N5Z1RUA
    A plant-derived surfactant made from natural sugars and fatty alcohols. It helps dissolve and mix ingredients evenly throughout the medicine, acting as an emulsifier and solubilizer in liquid formulations.
  • UNII B1K89384RJ
    A mixture of fatty alcohols derived from natural oils or fats, typically containing 14 to 22 carbon atoms. Used as an emollient, thickener, and emulsifier to improve texture and help blend oil and water components in formulations.
  • UNII UPY805K99W
    A synthetic compound derived from caprylic acid that works as a preservative and antimicrobial agent to help prevent bacterial and fungal growth in the medicine.
  • UNII N7YC58165T
    A synthetic polymer made from glycerin and sebacic acid, used as a film-former and binder in medications. It helps hold tablet or capsule ingredients together and may coat the product for controlled release.
  • UNII 00YIU5438U
    Caprylyl glycol is a clear liquid derived from coconut oil. In medicines, it acts as a humectant to retain moisture, a preservative booster to prevent microbial growth, and a solvent to help dissolve or mix other ingredients.
  • UNII 936JST6JCN
    Cetyl alcohol is a waxy, fatty substance derived from plant or animal sources. It acts as an emulsifier and thickener in medicines, helping blend oil and water components and giving products a smooth, creamy texture.
  • UNII RYQ4R60M02
    A green algae ingredient used as a natural colorant and nutritional filler in supplements and medications. It adds color and bulk to tablets and capsules.
  • 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 8D9H4QU99H
    A synthetic fatty acid ester derived from coconut oil, used as an emulsifier and solubilizer to help mix oil and water-based ingredients and improve how the body absorbs certain drugs.
  • UNII 1E5KJY107T
    A liquid mixture derived from coconut oil, coconut alkanes serve as a solvent and lubricant in medicines. They help dissolve active ingredients and reduce friction during manufacturing and tablet compression.
  • UNII 609A3V1SUA
    A silky liquid derived from caprylic acid that acts as an emollient and solvent in formulations. It helps dissolve active ingredients and improves the spreadability and feel of lotions, creams, and topical products.
  • UNII 5SL0G7R0OK
    A simple sugar made from corn or other plants, used in medicines as a filler and sweetener. It helps create the right texture and taste in tablets, powders, and liquid formulations.
  • UNII GAN16C9B8O
    Glutathione is a naturally occurring antioxidant compound made from three amino acids. In medications, it may serve as an antioxidant to protect the drug's active ingredients from breaking down or degrading over time.
  • UNII S9W6Z48HUP
    A synthetic compound made by chemically combining glycerin with other molecules. It works as a humectant and emollient in topical products, helping to soften skin and retain moisture in creams or ointments.
  • UNII PDC6A3C0OX
    Glycerin is a clear, thick liquid derived from plant oils or fats. It acts as a humectant to retain moisture, a sweetener, and a solvent in medications.
  • UNII WZ7DY7GBV6
    A plant-based oil extract from soybeans that contains compounds resistant to saponification. Used in formulations as an emollient and skin-conditioning agent to improve texture and spreadability of topical or oral products.
  • UNII 2788Z9758H
    A plant extract from licorice root used as a sweetener, flavoring agent, and natural emulsifier in medicines. It helps improve taste and may aid in keeping ingredients evenly mixed throughout the product.
  • UNII R9N3379M4Z
    Sunflower seed is a plant-derived ingredient used as a filler and source of oil in medications. It helps add bulk to the formulation and may serve as a natural binding or lubricating component.
  • UNII 42DG15CHXV
    A natural plant wax derived from sunflower seeds. It serves as a lubricant and glidant to help powders flow smoothly during manufacturing and tablet formation.
  • UNII J9JP2XE45M
    Hydrolyzed rice protein is a plant-derived ingredient made by breaking down rice protein into smaller fragments. It functions as a binder and texture agent, helping hold tablet ingredients together and improving product consistency.
  • UNII 8QWM6I035C
    A synthetic compound derived from myristic acid and nicotinic acid. It works as an emollient and skin-conditioning agent in topical formulations, helping to soften and smooth the product's texture on application.
  • UNII R60QEP13IC
    Rice bran is a natural powder made from the outer layer of rice grains. It's used in medicines as a filler and flow agent to add bulk and help the product mix and flow smoothly during manufacturing.
  • UNII 50C1307PZG
    Pentylene glycol is a humectant and preservative helper derived from petroleum or plant sources. It draws moisture into the product and helps prevent bacterial growth, keeping medicines stable during storage.
  • UNII HIE492ZZ3T
    Phenoxyethanol is a synthetic preservative and antimicrobial agent used to prevent bacterial and fungal growth in medicines and cosmetic products, extending shelf life and maintaining product safety.
  • UNII Q7UI015FF9
    A synthetic polymer material used as a thickener and stabilizer in liquid formulations. It helps create the right texture and prevents separation of ingredients in medicines and topical products.
  • UNII 46P231IQV8
    A synthetic emulsifier derived from glycerin and fatty acids. It helps blend oil and water-based ingredients together in cosmetic and pharmaceutical formulations to create stable, uniform products.
  • UNII W19EIO0DBE
    A plant-derived emulsifier made from glycerin and fatty acids. It helps mix oil and water-based ingredients together and stabilizes the product's texture in creams, lotions, and other cosmetic or topical formulations.
  • UNII 03KCY6P7UT
    A waxy compound derived from cetyl alcohol and phosphoric acid. It acts as an emulsifier to help blend oil and water ingredients, and as a thickener to give the medicine its proper texture and consistency.
  • UNII CI71S98N1Z
    A mineral salt containing potassium and phosphate, used as a buffer to help maintain the medicine's pH level and stability during storage.
  • UNII 5965N8W85T
    Propanediol is a clear liquid organic compound derived from vegetable sources or synthesized chemically. It acts as a humectant to retain moisture, a solvent to dissolve active ingredients, and a preservative booster in liquid medications and supplements.
  • UNII 3Z252A2K9G
    A natural ingredient derived from almond nuts. It's used as a flavoring agent and texture enhancer in medicines to improve taste and make the product more palatable.
  • UNII 7N2B70SFEZ
    Rice germ is the nutrient-rich inner layer of the rice grain. It's used in medicines as a filler and bulking agent to add volume and help bind ingredients together in tablets and capsules.
  • UNII 8LGU7VM393
    Rosemary leaf oil is a natural aromatic oil extracted from rosemary plants. It's used in medicines as a flavoring agent and preservative to help protect the product from spoilage.
  • UNII OJ245FE5EU
    Sodium benzoate is a salt derived from benzoic acid, a preservative. It's added to medicines to prevent growth of bacteria, fungi, and other microorganisms that could spoil the product.
  • UNII MD83SFE959
    A volatile organic liquid used as a solvent and preservative in medications. It helps dissolve active ingredients and other components, and can improve product stability and shelf life.
  • UNII MP1J8420LU
    A salt derived from edetic acid that binds to trace metals in medicines. It serves as a chelating agent and preservative to prevent metal-catalyzed breakdown of the drug and extend shelf life.
  • UNII R0ZB2556P8
    Tocopherol is a form of vitamin E derived from plant oils. It acts as an antioxidant in medicines to prevent oils and fats from breaking down and spoiling during storage.
  • UNII YA22H34H9Q
    A chelating agent derived from sodium and organic compounds. It binds to metal ions in the formulation to improve stability and prevent unwanted chemical reactions that could degrade the medicine.
  • UNII 059QF0KO0R
    Water is a liquid solvent that dissolves and mixes ingredients together in liquid medicines, syrups, and injections. It helps distribute the active drug evenly throughout the product.
  • UNII 44FQ49X6UN
    A polysaccharide (complex carbohydrate) derived from yeast cell walls. In medicines, it acts as a binder to hold tablet ingredients together and may help with tablet structure and stability.

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

The official label also statesWater (Aqua), Propanediol, Glycereth-7 Triacetate, Dicaprylyl Carbonate, Coconut Alkanes, Capryloyl Glycerin/Sebacic Acid Copolymer, Glycerin, Hydrolyzed Rice Protein, C14-22 Alcohols, Myristyl Nicotinate, Heptapeptide-68 Amide Acetate, Pentapeptide-84 Amide Acetate, Collagen Amino Acids, Glutathione, Chlorella Vulgaris Extract, Oryza Sativa (Rice) Extract, Oryza Sativa (Rice) Germ Extract, Prunus Amygdalus Dulcis (Sweet Almond) Seed Extract, Glycyrrhiza Glabra (Licorice) Root Extract, Oryza Sativa (Rice) Bran Extract, Rosmarinus Officinalis (Rosemary) Leaf Extract, Beta-Glucan, Coco-Caprylate/Caprate, Potassium Cetyl Phosphate, 1,2-Hexanediol, Glycine Soja (Soybean) Oil, Brassica Campestris (Rapeseed) Seed Oil, Helianthus Annuus (Sunflower) Seed Wax, C12-20 Alkyl Glucoside, Polyacrylate Crosspolymer-6, Polyglyceryl-3 Diisostearate, Polyglyceryl-3 Methylglucose Distearate, Caprylhydroxamic Acid, Helianthus Annuus (Sunflower) Extract, Acrylates/C10-30 Alkyl Acrylate Crosspolymer, Trisodium Ethylenediamine Disuccinate, Pentylene Glycol, Tocopherol, Cetyl Alcohol, Aminomethyl Propanol, Althaea Officinalis Root Extract, Dipotassium Phosphate, Caprylyl Glycol, t-Butyl Alcohol, Sodium Benzoate, Glucose, Citric Acid, Alcohol, Tetrasodium EDTA, Phenoxyethanol, Fragrance (Parfum) [ILN 25612]

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 gPer 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: 10 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
StriVectin TL Advanced Tightening Neck and Chest Broad Spectrum SPF 35 Sunscreen 3 g/100mL; 10 g/100mL; 7 g/100mL; 4.5 g/100mLthis 76147-0400-45 StriVectin 1 bottle — — 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

🏛️
2026
On the market since
Jan 2026
📍
2026
Currently FDA-listed
listed with the FDA
🔒
·
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.

📦 Packaging — all sizes for this product

Package NDCDescription Marketing startStatus
76147-0400-10 1 BOTTLE, PUMP in 1 CARTON (76147-400-10) / 10 mL in 1 BOTTLE, PUMP 2026-01-15 Active
76147-0400-45 You're viewing this 1 BOTTLE, PUMP in 1 CARTON (76147-400-45) / 45 mL in 1 BOTTLE, PUMP 2026-01-15 Active

Pack size FAQ

What quantity is in NDC 76147-0400-45?
NDC 76147-0400-45 is listed by the FDA — 1 bottle, pump in 1 carton / 45 ml in 1 bottle, pump.
What NDC number is used to bill for this package of StriVectin TL Advanced Tightening Neck and Chest Broad Spectrum SPF 35 Sunscreen Octocrylene, Homosalate, Octisalate, Avobenzone 3 g/100mL; 10 g/100mL; 7 g/100mL; 4.5 g/100mL Cream?
Bill NDC 76147-0400-45 — the 11-digit billing format is 76147040045. 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 76147-400-45, 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: 76147-0400-45, written without dashes as 76147040045. 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 76147-0400-45, the first segment (76147) is the labeler code FDA assigned to StriVectin Operating Company, Inc.; the middle segment (0400) identifies this specific product — its ingredient, strength, and dosage form; and the last segment (45) 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 StriVectin Operating Company, Inc.. 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 1 other package presentation of this same product, including 1 bottle (76147-0400-10). 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?
StriVectin Operating Company, Inc. 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 4 words ▾

Uses helps prevent sunburn

⏱️ Dosage and Administration 93 words ▾

Directions apply generously 15 minutes before sun exposure children under 6 months of age: Ask a doctor reapply at least every 2 hours use a water resistant sunscreen if swimming or sweating 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. to 2 p.m. wear long-sleeved shirts, pants, hats, and sunglasses

⚠️ Warnings 54 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 Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

📦 Storage and Handling 14 words ▾

Other Information protect the product in this container from excessive heat and direct sun.

🧪 Active Ingredient 10 words ▾

Active Ingredients Avobenzone 3.0% Homosalate 7.0% Octisalate 4.5% Octocrylene 10.0%

🧪 Inactive Ingredients 140 words ▾

Inactive Ingredients Water (Aqua), Propanediol, Glycereth-7 Triacetate, Dicaprylyl Carbonate, Coconut Alkanes, Capryloyl Glycerin/Sebacic Acid Copolymer, Glycerin, Hydrolyzed Rice Protein, C14-22 Alcohols, Myristyl Nicotinate, Heptapeptide-68 Amide Acetate, Pentapeptide-84 Amide Acetate, Collagen Amino Acids, Glutathione, Chlorella Vulgaris Extract, Oryza Sativa (Rice) Extract, Oryza Sativa (Rice) Germ Extract, Prunus Amygdalus Dulcis (Sweet Almond) Seed Extract, Glycyrrhiza Glabra (Licorice) Root Extract, Oryza Sativa (Rice) Bran Extract, Rosmarinus Officinalis (Rosemary) Leaf Extract, Beta-Glucan, Coco-Caprylate/Caprate, Potassium Cetyl Phosphate, 1,2-Hexanediol, Glycine Soja (Soybean) Oil, Brassica Campestris (Rapeseed) Seed Oil, Helianthus Annuus (Sunflower) Seed Wax, C12-20 Alkyl Glucoside, Polyacrylate Crosspolymer-6, Polyglyceryl-3 Diisostearate, Polyglyceryl-3 Methylglucose Distearate, Caprylhydroxamic Acid, Helianthus Annuus (Sunflower) Extract, Acrylates/C10-30 Alkyl Acrylate Crosspolymer, Trisodium Ethylenediamine Disuccinate, Pentylene Glycol, Tocopherol, Cetyl Alcohol, Aminomethyl Propanol, Althaea Officinalis Root Extract, Dipotassium Phosphate, Caprylyl Glycol, t-Butyl Alcohol, Sodium Benzoate, Glucose, Citric Acid, Alcohol, Tetrasodium EDTA, Phenoxyethanol, Fragrance (Parfum) [ILN 25612]

🎯 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 ↗
← 76147-0301-07 · StriVectin 76151-0105-11 · Boscia →
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.