Home › NDC Lookup › Ingredients › Avobenzone Homosalate Octisalate Octocry... › 74472-0501-02
SOME BY MI TRUECICA AQUA CALMING SUNSCREEN Avobenzone, Homosalate, Octisalate, Octocrylene 2.4 g/50mL; 3.65 g/50mL; 1.5 g/50mL; 4.35 g/50mL Cream — NDC 74472-0501-02 package photo

SOME BY MI TRUECICA AQUA CALMING SUNSCREEN Avobenzone, Homosalate, Octisalate, Octocrylene 2.4 g/50mL; 3.65 g/50mL; 1.5 g/50mL; 4.35 g/50mL Cream

by PERENNEBELL Co., Ltd. · 1 TUBE in 1 BOX (74472-501-02) / 50 mL in 1 TUBE (74472-501-01)
NDC 74472-0501-02
🏷️ FDA NDC (as labeled) 74472-501-02 billing pads the product segment with a zero
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) 74472-501-02
Product NDC 74472-501
11-digit billing NDC 74472050102
UNII 4X49Y0596W, V06SV4M95S, G63QQF2NOX, 5A68WGF6WM
Application # M020
SPL Set ID 4d42d5aa-d12e-1086-e063-6294a90a12df
DEA schedule Non-controlled
Marketing category OTC MONOGRAPH DRUG
Marketing status On market
FDA listing status Listed (active directory)
Marketing start 2026-04-01
Route TOPICAL
Dosage form CREAM
Substance OCTISALATE; HOMOSALATE; AVOBENZONE; OCTOCRYLENE
Why two NDCs? The FDA registers this code as 74472-501-02 — 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 → 74472-0501-02. 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

LabelerPERENNEBELL Co., Ltd.
FDA applicationM020 (OTC MONOGRAPH DRUG)
Labeler code74472
First marketedApr 2026
Product typeHuman Otc Drug
Portfolio4 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?

This is a topical cream sunscreen marketed as an over-the-counter monograph product. It contains four UV-filtering agents (avobenzone, homosalate, octisalate, and octocrylene) that are typically used together to absorb and scatter ultraviolet radiation from the sun. Products with these ingredients are commonly applied to skin to help reduce sun exposure and protect against UV-related damage.

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 K72T3FS567
    Adenosine is a naturally occurring nucleoside compound. In medicines, it functions as an active pharmaceutical ingredient in some formulations, though when listed as an excipient it may serve as a buffering or stabilizing agent to maintain product stability and pH.
  • UNII ZY81Z83H0X
    Aloe vera leaf is a plant extract derived from the aloe plant. It is used in medicines as a natural moisturizer and skin-soothing agent in topical formulations.
  • UNII W59H9296ZG
    A synthetic polymer made from acrylic compounds and vinylpyrrolidone. It works as a film-former and thickener in topical products, helping create a smooth texture and improve how the medication spreads on skin.
  • UNII 94ZLA3W45F
    Arginine is an amino acid used in medicines as a buffer and pH adjuster. It helps maintain the proper acidity level and stability of liquid formulations.
  • UNII 852FKP35KV
    A plant extract from artemisia capillaris, used as a natural flavoring or coloring agent in some medicines. It may help give the product taste, aroma, or appearance.
  • UNII 9PA5A687X5
    Asiatic acid is a natural compound extracted from plants that acts as an emollient and skin-conditioning agent in topical formulations. It helps soften and smooth the product's texture while supporting skin hydration.
  • UNII PKO39VY215
    A natural compound derived from Centella asiatica plant, used as an active botanical extract or skin-conditioning agent in topical formulations to support ingredient stability and product efficacy.
  • UNII 3XUS85K0RA
    Butylene glycol is a clear liquid derived from petroleum or plants that acts as a humectant, solvent, and preservative booster in medicines. It helps keep formulations stable, dissolve active ingredients, and maintain moisture in topical products.
  • 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 0A5MM307FC
    A synthetic polymer that absorbs water and forms a thick, gel-like substance. In medicines, it works as a thickener and stabilizer to improve texture and help ingredients stay mixed together in creams, gels, and lotions.
  • UNII 7M867G6T1U
    Centella asiatica is a plant extract used in medicines as a skin-conditioning or soothing ingredient. It helps maintain product stability and may support skin comfort in topical formulations.
  • UNII 58B69Q84JO
    A plant-derived emulsifier made from olive oil and fatty alcohols. It helps blend oil and water ingredients together and stabilizes the product's texture in creams, lotions, and similar formulations.
  • UNII QYO8Q067D0
    Citronella oil is a natural plant-derived oil used as a fragrance and flavoring agent in medicines. It provides taste and aroma to make medications more palatable for patients.
  • UNII F4K100DXP3
    Dibutyl adipate is a synthetic oily liquid derived from adipic acid. It serves as a plasticizer and solvent in medicines, helping softens coatings and improves flexibility so tablets and capsules don't crack or break.
  • UNII E107L85C40
    Dipropylene glycol is a clear liquid made from propylene glycol. It acts as a solvent and humectant in medicines, helping dissolve active ingredients and retain moisture in the formulation.
  • UNII M9JGK7U88V
    Ethohexadiol is a synthetic alcohol used as a preservative and antimicrobial agent in medicines. It helps prevent bacterial and fungal growth to keep the product stable and safe during storage.
  • UNII 147D247K3P
    Ethylhexylglycerin is a synthetic preservative used to prevent bacteria and mold from growing in medicines and personal care products. It helps keep the product safe and stable throughout its shelf life.
  • 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 FCZ5MH785I
    A waxy substance made from glycerin and stearic acid. It works as an emulsifier to help mix oil and water ingredients together, and as a thickener to give the medicine its proper texture and consistency.
  • UNII U2585P4K7Y
    A skin-conditioning agent derived from hyaluronic acid that has been broken down into smaller molecules. It's used in topical products to help moisturize and smooth the skin surface.
  • UNII 918X1OUF1E
    Isohexadecane is a synthetic hydrocarbon oil used as an emollient and solvent in topical medicines. It helps dissolve active ingredients and improves spreadability and absorption through the skin.
  • UNII ZBP1YXW0H8
    A fragrant oil extracted from lavender plants, used as a flavoring and scent agent in medicines to improve taste and aroma.
  • UNII 2XIW34BN6O
    A fragrant oil derived from litsea cubeba fruit, used as a flavoring agent and aromatic ingredient to improve the taste and smell of the medicine.
  • UNII M7O1N24J82
    Madecassic acid is a natural compound extracted from Centella asiatica plant. In medications, it acts as an active pharmaceutical ingredient or functional excipient that may support skin health and wound healing in topical formulations.
  • UNII CQ2F5O6YIY
    A natural compound extracted from Centella asiatica plant used as an active skin-conditioning ingredient. It functions as a humectant and skin protectant to improve moisture retention and support skin barrier function in topical formulations.
  • UNII G43C57162K
    A natural plant extract from tea tree leaves used in topical formulations. It acts as a fragrance, preservative, and antimicrobial agent to help maintain product freshness and sensory appeal.
  • UNII 46477RRB3O
    A plant material from spearmint used as a natural flavoring and aromatic agent. It provides a minty taste and cooling sensation to improve the medicine's palatability.
  • UNII N8F53B3R4R
    A synthetic humectant and solvent derived from propane. It draws and holds moisture in the formulation, helping keep the medicine stable and improving texture or flow in liquid and semi-solid products.
  • UNII 25X51I8RD4
    Niacinamide is a form of vitamin B3, a water-soluble nutrient. In medicines, it may be added as a nutritional supplement or to support skin health, though its primary role here is as an active ingredient rather than a traditional inactive filler.
  • UNII 40KQ7Q535O
    A plant extract from white water lily flowers. It's used in formulations for its soothing and skin-conditioning properties, often included in topical products as a natural ingredient to enhance texture and feel.
  • UNII Z129UMU8LE
    A fragrant oil extracted from basil leaves, used as a flavoring agent to improve taste and provide the characteristic aroma in medicines.
  • UNII WV9CM0O67Z
    Panthenol is a humectant and skin-conditioning agent derived from pantothenic acid. It's added to medicines to help retain moisture and soothe skin irritation.
  • 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 4T2L7QI313
    A waxy, plant-derived thickener made from glycerol and behenic acid. It's used as an emulsifier and stabilizer to help blend oil and water-based ingredients together and maintain texture in creams and lotions.
  • UNII ETY9Q81E2T
    A synthetic emulsifier made from glycerin and stearic acid. It helps blend oil and water-based ingredients together so the medicine mixes evenly and stays stable.
  • UNII D5J3623SV2
    Portulaca oleracea is a plant extract used in medicines as a natural ingredient. It may function as an antioxidant or skin-conditioning agent in topical formulations.
  • 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 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 C7X2ALW7JZ
    A plant extract derived from the whole saussurea involucrata plant. It is used in formulations as a flavoring agent or natural ingredient to add botanical character to the medicine.
  • UNII 64L053FRFO
    Sodium palmitoyl proline is a synthetic compound made from the amino acid proline combined with palmitic acid (a fatty acid). It acts as an emulsifier and skin-conditioning agent in topical formulations, helping mix oil and water components and maintain product texture.
  • 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 5776GCL1DG
    A synthetic compound made by combining stearic acid (a fatty substance) with polyethylene glycol. It acts as an emulsifier and solubilizer to help mix oil and water ingredients together in the medicine.
  • UNII 8L72OKJ7II
    A plant extract from common thyme used as a flavoring agent and preservative in medicines. It adds taste and helps protect the product from spoilage.
  • 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 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.
  • UNII 9NH1UDD2RR
    A synthetic silicone polymer that forms a smooth, water-resistant film. Used in topical formulations as a skin protectant coating and to improve product texture and spreadability on the skin.
  • 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.

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

The official label also statesWater, Butylene Glycol, Polyglyceryl-6 Stearate, Dibutyl Adipate, Isohexadecane, Niacinamide, Pentylene Glycol, Glyceryl Stearate SE, Arginine, Cetearyl Olivate, Acrylates/C10-30 Alkyl Acrylate Crosspolymer, Polyglyceryl-6 Behenate, Sorbitan Olivate, Carbomer, 1,2-Hexanediol, Vinyl Dimethicone/Methicone Silsesquioxane Crosspolymer, Ammonium Acryloyldimethyltaurate/VP Copolymer, Methylpropanediol, Adenosine, Ethylhexylglycerin, Caprylyl Glycol, Rosmarinus Officinalis (Rosemary) Leaf Oil, Mentha Arvensis Extract, Ethyl Hexanediol, Tocopherol, Trehalose, Melaleuca Alternifolia (Tea Tree) Leaf Water, Centella Asiatica Extract, Hydrolyzed Hyaluronic Acid, Panthenol, Cymbopogon Nardus (Citronella) Oil, Dipropylene Glycol, Lavandula Angustifolia (Lavender) Oil, Aloe Barbadensis Leaf Extract, Ocimum Basilicum (Basil) Oil, Litsea Cubeba Fruit Oil, Propanediol, Sodium Palmitoyl Proline, Steareth-30, Artemisia Capillaris Extract, Glycerin, Saussurea Involucrata Extract, Portulaca Oleracea Extract, Madecassoside, Asiaticoside, Thymus Vulgaris (Thyme) Extract, Madecassic Acid, Asiatic Acid, Nymphaea Alba Flower Extract

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.
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
Some By Mi Truecica Aqua Calming Sunscreen 2.4 g/50mL; 3.65 g/50mL; 1.5 g/50mL; 4.35 g/50mLthis 74472-0501-02 PERENNEBELL 1 tube — — 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
Apr 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
74472-0501-02 You're viewing this 1 TUBE in 1 BOX (74472-501-02) / 50 mL in 1 TUBE (74472-501-01) 2026-04-01 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 74472-501-02, 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: 74472-0501-02, written without dashes as 74472050102. 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 74472-0501-02, the first segment (74472) is the labeler code FDA assigned to PERENNEBELL Co., Ltd.; the middle segment (0501) identifies this specific product — its ingredient, strength, and dosage form; and the last segment (02) 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 PERENNEBELL Co., Ltd.. Listing status can change — the directory data on this page refreshes weekly.
Who lists this product with the FDA?
PERENNEBELL Co., Ltd. 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 🧪 Active Ingredient 🧪 Inactive Ingredients 🎯 Purpose
🎯 Indications and Usage 32 words ▾

Uses ■ Helps prevent sun burn. ■ 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 99 words ▾

Directions ■ Apply liberally 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. – 2 p.m. • wear long-sleeved shirts, pants, hats, and sunglasses.

⚠️ Warnings 5 words ▾

Warnings For external use only

🧪 Active Ingredient 14 words ▾

Active ingredients Avobenzone 2.8 %, Homosalate 7.3 %, Octisalate 4.8 %, Octocrylene 8.7 %

🧪 Inactive Ingredients 117 words ▾

Inactive ingredients Water, Butylene Glycol, Polyglyceryl-6 Stearate, Dibutyl Adipate, Isohexadecane, Niacinamide, Pentylene Glycol, Glyceryl Stearate SE, Arginine, Cetearyl Olivate, Acrylates/C10-30 Alkyl Acrylate Crosspolymer, Polyglyceryl-6 Behenate, Sorbitan Olivate, Carbomer, 1,2-Hexanediol, Vinyl Dimethicone/Methicone Silsesquioxane Crosspolymer, Ammonium Acryloyldimethyltaurate/VP Copolymer, Methylpropanediol, Adenosine, Ethylhexylglycerin, Caprylyl Glycol, Rosmarinus Officinalis (Rosemary) Leaf Oil, Mentha Arvensis Extract, Ethyl Hexanediol, Tocopherol, Trehalose, Melaleuca Alternifolia (Tea Tree) Leaf Water, Centella Asiatica Extract, Hydrolyzed Hyaluronic Acid, Panthenol, Cymbopogon Nardus (Citronella) Oil, Dipropylene Glycol, Lavandula Angustifolia (Lavender) Oil, Aloe Barbadensis Leaf Extract, Ocimum Basilicum (Basil) Oil, Litsea Cubeba Fruit Oil, Propanediol, Sodium Palmitoyl Proline, Steareth-30, Artemisia Capillaris Extract, Glycerin, Saussurea Involucrata Extract, Portulaca Oleracea Extract, Madecassoside, Asiaticoside, Thymus Vulgaris (Thyme) Extract, Madecassic Acid, Asiatic Acid, Nymphaea Alba Flower Extract

🎯 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 ↗
← 74472-0235-01 · PERENNEBELL 74472-0701-02 · PERENNEBELL →
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.