Neutrogena Revitalizing Lip Balm Broad Spectrum SPF 20 - Fresh Plum 60 Avobenzone, Homosalate, Octocrylene 30 mg/g; 60 mg/g; 100 mg/g Stick, 1 canister — NDC 69968-0887-01 package photo

Neutrogena Revitalizing Lip Balm Broad Spectrum SPF 20 - Fresh Plum 60 Avobenzone, Homosalate, Octocrylene 30 mg/g; 60 mg/g; 100 mg/g Stick, 1 canister

by Kenvue Brands LLC · 1 CANISTER in 1 BLISTER PACK (69968-0887-1) / 4.2 g in 1 CANISTER
NDC 69968-0887-01
🏷️ FDA NDC (as labeled) 69968-0887-1 billing pads the package segment with a zero
OTC On market Non-controlled
🗂️ Data synced Sep 17, 2026 · sources: openFDA · FDA label (DailyMed) · FDA Orange & Purple Book · First Databank · CMS NADAC, ASP, Medicare & Medicaid · RxNorm
📋 All sources & update times →

🆔 Identity & classification

FDA NDC (as labeled) 69968-0887-1
Product NDC 69968-0887
11-digit billing NDC 69968088701
UNII G63QQF2NOX, V06SV4M95S, 5A68WGF6WM
UPC 0086800009658, 0086800009610, 0086800009641, 0086800009627 +2 more
Application # M020
SPL Set ID 16ac7877-8dfd-3d69-e063-6394a90a5a8a
DEA schedule Non-controlled
Marketing category OTC MONOGRAPH DRUG
Marketing status On market
FDA listing status Listed (active directory)
Marketing start 2024-05-15
Route TOPICAL
Dosage form STICK
Substance AVOBENZONE; HOMOSALATE; OCTOCRYLENE
Why two NDCs? The FDA registers this code as 69968-0887-1 — a 5-4-1 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 package segment → 69968-0887-01. 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

LabelerKenvue Brands LLC
FDA applicationM020 (OTC MONOGRAPH DRUG)
Labeler code69968
First marketedMay 2024
Product typeHuman Otc Drug
Portfolio564 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?

Neutrogena Revitalizing Lip Balm Broad Spectrum SPF 20 is a topical stick product containing three sunscreen active ingredients: avobenzone, homosalate, and octocrylene. These ingredients function as ultraviolet light filters that are commonly used in sunscreen products to help protect skin from sun exposure. This is an over-the-counter monograph drug, meaning it is marketed under FDA's established rules for sunscreen products rather than as an individually reviewed application.

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 G27BTQ95MJ
    A plant-derived waxy compound made from oils and alcohols. It acts as an emulsifier and texture agent, helping blend water and oil components together and giving the medicine a smooth, stable consistency.
  • 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 Q1LS2UJO3A
    Ceresin is a purified mineral wax derived from ozocerite. It functions as a binding agent, thickener, and coating material in medicines to help hold ingredients together and provide texture or protective coating.
  • UNII A7EVH2RK4O
    Cetyl lactate is a waxy compound made from lactic acid and cetyl alcohol. It works as an emulsifier and thickener to help mix oil and water ingredients and give the medicine the right texture.
  • UNII ECW0LZ41X8
    A synthetic red dye used to color tablets and capsules. It helps make medicines visually distinctive so patients can easily identify their medication.
  • UNII I0DQJ7YGXM
    A synthetic chemical compound used as a plasticizer in pharmaceutical coatings. It makes film coatings more flexible and durable so they don't crack or peel during manufacturing and storage.
  • UNII 2865993309
    Ethylhexyl palmitate is an oily chemical made from palm oil and alcohol. It acts as an emollient and skin-conditioning agent in topical medicines, helping the product spread smoothly and keeping skin soft.
  • 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 7D1YQ9Y5EZ
    Hydrogenated polybutene is a thick, wax-like ingredient made by chemically processing petroleum. It acts as a binder and lubricant, helping hold tablet ingredients together and allowing pills to slide smoothly during manufacturing and packaging.
  • UNII 949E3KBJ1I
    Isopropyl titanium triisostearate is a titanium-based compound used in medicines as a glidant and anticaking agent. It helps powders and granules flow smoothly during manufacturing and prevents clumping in the finished product.
  • UNII 884C3FA9HE
    Lanolin alcohol is a waxy substance derived from sheep's wool. It functions as an emollient and emulsifier in medicines, helping blend oil and water-based ingredients while softening the product's texture.
  • 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 4042ZC00DY
    A waxy ester derived from myristic acid, used as an emollient and lubricant in topical formulations. It helps soften skin contact, reduce friction during application, and improve the texture and spreadability of creams and ointments.
  • UNII RV743D216M
    A synthetic peptide derived from fatty acids and amino acids. It functions as a skin-conditioning agent and emollient in topical formulations, helping soften and smooth the product texture while supporting skin hydration.
  • UNII 255PIF62MS
    A synthetic antioxidant compound used to prevent oils and fats in medications from breaking down or becoming rancid during storage. It helps maintain the medicine's stability and shelf life.
  • UNII 4T6H12BN9U
    Petrolatum is a purified mineral oil-based jelly derived from petroleum. In medicines, it acts as an emollient, lubricant, and moisture barrier to soften skin, reduce friction, and help prevent water loss from formulations.
  • UNII DR0K5NOJ4R
    Phenyl trimethicone is a silicone-based lubricant and glidant. It helps powder particles flow smoothly and reduces friction during tablet or capsule manufacturing and filling.
  • UNII 1NA5AO9GH7
    A synthetic polymer derived from petroleum, polybutene is used as a binder and lubricant in solid medications to help hold ingredients together and improve the tablet or capsule's flow during manufacturing.
  • UNII K49155WL9Y
    Shea butter is a fat extracted from shea tree nuts. It's used in medicines as an emollient and lubricant to soften the product, improve texture, and help ingredients blend smoothly together.
  • 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 01S2G2C1E4
    Sorbitan isostearate is an emulsifier derived from sorbitol and isostearic acid. It helps mix oil and water-based ingredients together and keeps them blended throughout the medicine's shelf life.
  • UNII 15FIX9V2JP
    Titanium dioxide is a bright white mineral powder commonly used as a colorant and opacifying agent. It makes pills and tablets white or lighter in color and helps make coatings non-transparent.
  • UNII 8OC9U7TQZ0
    Tribehenin is a waxy, plant-derived substance that acts as a lubricant and glidant in tablets and capsules. It helps the medicine flow smoothly during manufacturing and prevents sticking during production and packaging.

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

The official label also statesHydrogenated Polyisobutene, Polybutene, Petrolatum, Phenyl Trimethicone, Ozokerite, Diethylhexyl 2,6-Naphthalate, Hydrogenated Lanolin, Synthetic Wax, Bis-Behenyl/Isostearyl/Phytosteryl Dimer Dilinoleyl Dimer Dilinoleate, Butyrospermum Parkii (Shea) Butter, Euphorbia Cerifera (Candelilla) Wax, Cetyl Lactate, Myristyl Myristate, Mica, Silica, Copernicia Cerifera (Carnauba) Wax, Stearoxymethicone/Dimethicone Copolymer, Ethylhexyl Palmitate, Tribehenin, Flavor, Fragrance, Silica Silylate, Pentaerythrityl Tetra-di-t-butyl Hydroxyhydrocinnamate, Sorbitan Isostearate, Isopropyl Titanium Triisostearate, Palmitoyl Tripeptide-1, Iron Oxides,Titanium Dioxide, Red 7 Lake Hydrogenated Polyisobutene, Petrolatum, Polybutene, Phenyl Trimethicone, Ozokerite, Diethylhexyl 2,6-Naphthalate, Hydrogenated Lanolin, Synthetic Wax, Bis-Behenyl/Isostearyl/Phytosteryl Dimer Dilinoleyl Dimer Dilinoleate, Butyrospermum Parkii (Shea) Butter, Euphorbia Cerifera (Candelilla) Wax, Cetyl Lactate, Myristyl Myristate, Silica, Copernicia Cerifera (Carnauba) Wax, Stearoxymethicone/Dimethicone Copolymer, Ethylhexyl Palmitate, Tribehenin, Flavor, Fragrance, Silica Silylate, Pentaerythrityl Tetra-di-t-butyl Hydroxyhydrocinnamate, Sorbitan Isostearate, Isopropyl Titanium Triisostearate, Palmitoyl Tripeptide-1, Iron Oxides,Titanium Dioxide, Red 7 Lake Hydrogenated Polyisobutene, Petrolatum, Polybutene, Phenyl Trimethicone, Ozokerite, Diethylhexyl 2,6-Naphthalate, Hydrogenated Lanolin, Synthetic Wax, Bis-Behenyl/Isostearyl/Phytosteryl Dimer Dilinoleyl Dimer Dilinoleate, Butyrospermum Parkii (Shea) Butter, Euphorbia Cerifera (Candelilla) Wax, Cetyl Lactate, Myristyl Myristate, Silica, Copernicia Cerifera (Carnauba) Wax, Stearoxymethicone/Dimethicone Copolymer, Ethylhexyl Palmitate, Tribehenin, Flavor, Fragrance, Silica Silylate, Pentaerythrityl Tetra-di-t-butyl Hydroxyhydrocinnamate, Sorbitan Isostearate, Isopropyl Titanium Triisostearate, Palmitoyl Tripeptide-1, Mica, Titanium Dioxide, Iron Oxides Hydrogenated Polyisobutene, Petrolatum, Polybutene, Phenyl Trimethicone, Ozokerite, Diethylhexyl 2,6-Naphthalate, Hydrogenated Lanolin, Synthetic Wax, Bis-Behenyl/Isostearyl/Phytosteryl Dimer Dilinoleyl Dimer Dilinoleate, Butyrospermum Parkii (Shea) Butter, Euphorbia Cerifera (Candelilla) Wax, Cetyl Lactate, Myristyl Myristate, Silica, Copernicia Cerifera (Carnauba) Wax, Stearoxymethicone/Dimethicone Copolymer, Ethylhexyl Palmitate, Tribehenin, Flavor, Fragrance, Silica Silylate, Pentaerythrityl Tetra-di-t-butyl Hydroxyhydrocinnamate, Sorbitan Isostearate, Isopropyl Titanium Triisostearate, Palmitoyl Tripeptide-1,Titanium Dioxide, Red 6 Lake, Red 7 Lake, Iron Oxides

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 DailyMedingredient 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.
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
Neutrogena Revitalizing Lip Balm Broad Spectrum SPF 20 - Sunny Berry 30 30 mg/g; 60 mg/g; 100 mg/g 69968-0886-01 Kenvue 1 canister FDA listed
Neutrogena Revitalizing Lip Balm Broad Spectrum SPF 20 - Fresh Plum 60 30 mg/g; 60 mg/g; 100 mg/gthis 69968-0887-01 Kenvue 1 canister 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

🏛️
2024
On the market since
May 2024
📍
2026
Currently FDA-listed
2 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.

📦 Packaging — all sizes for this product

Package NDCDescription Marketing startStatus
69968-0887-01 You're viewing this 1 CANISTER in 1 BLISTER PACK (69968-0887-1) / 4.2 g in 1 CANISTER 2024-05-15 Active

🧭 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 69968-0887-1, 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: 69968-0887-01, written without dashes as 69968088701. 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 69968-0887-01, the first segment (69968) is the labeler code FDA assigned to Kenvue Brands LLC; the middle segment (0887) identifies this specific product — its ingredient, strength, and dosage form; and the last segment (01) 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 Kenvue Brands LLC. Listing status can change — the directory data on this page refreshes weekly.
Who lists this product with the FDA?
Kenvue Brands 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 126 words

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

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

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

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 ~2 min read

Directions ■ apply generously 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 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 ■ children under 6 months of age: Ask a doctor

Directions ■ apply generously 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 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 ■ children under 6 months of age: Ask a doctor

Directions ■ apply generously 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 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■ children under 6 months of age: Ask a doctor

Directions ■ apply generously 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 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 ■ children under 6 months of age: Ask a doctor

⚠️ Warnings ~1 min read

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.

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

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

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 66 words

Other information protect this product from excessive heat and direct sun may stain some fabrics

Other information ■ protect this product from excessive heat and direct sun ■ may stain some fabrics

Other information ■ protect this product from excessive heat and direct sun ■ may stain some fabrics

Other information ■ protect this product from excessive heat and direct sun ■ may stain some fabrics

🧪 Active Ingredient 32 words

Active ingredients Avobenzone (3%), Homosalate (6%), Octocrylene (10%)

Active ingredients Avobenzone (3%), Homosalate (6%), Octocrylene (10%)

Active ingredients Avobenzone (3%), Homosalate (6%), Octocrylene (10%)

Active ingredients Avobenzone (3%), Homosalate (6%), Octocrylene (10%)

🧪 Inactive Ingredients ~1 min read

Inactive ingredients Hydrogenated Polyisobutene, Polybutene, Petrolatum, Phenyl Trimethicone, Ozokerite, Diethylhexyl 2,6-Naphthalate, Hydrogenated Lanolin, Synthetic Wax, Bis-Behenyl/Isostearyl/Phytosteryl Dimer Dilinoleyl Dimer Dilinoleate, Butyrospermum Parkii (Shea) Butter, Euphorbia Cerifera (Candelilla) Wax, Cetyl Lactate, Myristyl Myristate, Mica, Silica, Copernicia Cerifera (Carnauba) Wax, Stearoxymethicone/Dimethicone Copolymer, Ethylhexyl Palmitate, Tribehenin, Flavor, Fragrance, Silica Silylate, Pentaerythrityl Tetra-di-t-butyl Hydroxyhydrocinnamate, Sorbitan Isostearate, Isopropyl Titanium Triisostearate, Palmitoyl Tripeptide-1, Iron Oxides,Titanium Dioxide, Red 7 Lake

Inactive ingredients Hydrogenated Polyisobutene, Petrolatum, Polybutene, Phenyl Trimethicone, Ozokerite, Diethylhexyl 2,6-Naphthalate, Hydrogenated Lanolin, Synthetic Wax, Bis-Behenyl/Isostearyl/Phytosteryl Dimer Dilinoleyl Dimer Dilinoleate, Butyrospermum Parkii (Shea) Butter, Euphorbia Cerifera (Candelilla) Wax, Cetyl Lactate, Myristyl Myristate, Silica, Copernicia Cerifera (Carnauba) Wax, Stearoxymethicone/Dimethicone Copolymer, Ethylhexyl Palmitate, Tribehenin, Flavor, Fragrance, Silica Silylate, Pentaerythrityl Tetra-di-t-butyl Hydroxyhydrocinnamate, Sorbitan Isostearate, Isopropyl Titanium Triisostearate, Palmitoyl Tripeptide-1, Iron Oxides,Titanium Dioxide, Red 7 Lake

Inactive ingredients Hydrogenated Polyisobutene, Petrolatum, Polybutene, Phenyl Trimethicone, Ozokerite, Diethylhexyl 2,6-Naphthalate, Hydrogenated Lanolin, Synthetic Wax, Bis-Behenyl/Isostearyl/Phytosteryl Dimer Dilinoleyl Dimer Dilinoleate, Butyrospermum Parkii (Shea) Butter, Euphorbia Cerifera (Candelilla) Wax, Cetyl Lactate, Myristyl Myristate, Silica, Copernicia Cerifera (Carnauba) Wax, Stearoxymethicone/Dimethicone Copolymer, Ethylhexyl Palmitate, Tribehenin, Flavor, Fragrance, Silica Silylate, Pentaerythrityl Tetra-di-t-butyl Hydroxyhydrocinnamate, Sorbitan Isostearate, Isopropyl Titanium Triisostearate, Palmitoyl Tripeptide-1, Mica, Titanium Dioxide, Iron Oxides

Inactive ingredients Hydrogenated Polyisobutene, Petrolatum, Polybutene, Phenyl Trimethicone, Ozokerite, Diethylhexyl 2,6-Naphthalate, Hydrogenated Lanolin, Synthetic Wax, Bis-Behenyl/Isostearyl/Phytosteryl Dimer Dilinoleyl Dimer Dilinoleate, Butyrospermum Parkii (Shea) Butter, Euphorbia Cerifera (Candelilla) Wax, Cetyl Lactate, Myristyl Myristate, Silica, Copernicia Cerifera (Carnauba) Wax, Stearoxymethicone/Dimethicone Copolymer, Ethylhexyl Palmitate, Tribehenin, Flavor, Fragrance, Silica Silylate, Pentaerythrityl Tetra-di-t-butyl Hydroxyhydrocinnamate, Sorbitan Isostearate, Isopropyl Titanium Triisostearate, Palmitoyl Tripeptide-1,Titanium Dioxide, Red 6 Lake, Red 7 Lake, Iron Oxides

🎯 Purpose 8 words

Purpose Sunscreen

Purpose Sunscreen

Purpose Sunscreen

Purpose Sunscreen

Source: FDA Structured Product Labeling, mirrored from DailyMed / openFDA. Prefer the government’s original formatting? View this label on DailyMed ↗
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.