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Oathology Inzincable Lip Balm SPF 35 ZINC OXIDE 150 mg/mL Ointment

by SKINOATH LLC · 1 TUBE in 1 BOX (85562-694-00) / 10 mL in 1 TUBE
NDC 85562-0694-00
🏷️ FDA NDC (as labeled) 85562-694-00 billing pads the product segment with a zero
OTC On market Non-controlled
🗂️ Data synced Jul 24, 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

⚠️
Other active recalls for Zinc Oxide (different manufacturers) — 6 · tap to view
These affect other manufacturers’ products for the same ingredient — not necessarily the exact NDC on this page.
Class II · Oct 31, 2025 — cGMP deviations (Blossom Pharmaceuticals) · FDA recall D-0212-2026
Class II · Oct 31, 2025 — cGMP deviations (Blossom Pharmaceuticals) · FDA recall D-0206-2026
Class II · Oct 31, 2025 — cGMP deviations (Blossom Pharmaceuticals) · FDA recall D-0202-2026
Class II · Oct 31, 2025 — cGMP deviations (Blossom Pharmaceuticals) · FDA recall D-0207-2026
Class II · Oct 31, 2025 — cGMP deviations (Blossom Pharmaceuticals) · FDA recall D-0209-2026
Class II · Oct 31, 2025 — cGMP deviations (Blossom Pharmaceuticals) · FDA recall D-0208-2026
Each entry is an official FDA enforcement report — look up any recall number in the FDA recall database ↗

🆔 Identity & classification

FDA NDC (as labeled) 85562-694-00
Product NDC 85562-694
11-digit billing NDC 85562069400
UNII SOI2LOH54Z
Application # M020
SPL Set ID 289a5492-af57-42e5-82af-3f1e4b369d68
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 2025-04-22
Route TOPICAL
Dosage form OINTMENT
Substance ZINC OXIDE
Why two NDCs? The FDA registers this code as 85562-694-00 — 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 → 85562-0694-00. 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

LabelerSKINOATH LLC
FDA applicationM020 (OTC MONOGRAPH DRUG)
Labeler code85562
First marketedApr 2025
Product typeHuman Otc Drug
Portfolio2 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?

Oathology Inzincable Lip Balm SPF 35 is a topical ointment containing zinc oxide, a mineral sunscreen agent. Zinc oxide is commonly used in lip balms and sunscreen products to help protect the skin from ultraviolet (UV) rays. This product is an over-the-counter monograph drug, meaning it is marketed under FDA's established rules for sunscreen products rather than through individual application review.

Supplement & herbal interactions

Some supplements/herbs that may interact with Zinc oxide (OTC drug) — tap one for details:

Dimethylsulfoxide (dmso)Moderate Turpentine OilModerate AlchemillaMinor
🌿 Every supplement checked against Zinc oxide (OTC drug) (3 interactions) — ranked by severity →
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 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 2EH13UN8D3
    A synthetic compound used as a solvent and penetration enhancer in topical formulations. It helps dissolve active ingredients and allows them to penetrate the skin more effectively.
  • UNII D5340Y2I9G
    Castor oil is a natural plant-based oil used in medicines as a lubricant, laxative agent, and solvent. It helps medicine ingredients dissolve or flow smoothly and can aid bowel movement in formulations designed for that purpose.
  • UNII 2S42T2808B
    A synthetic red dye used as a colorant to give the medicine its red color. It helps make pills or liquids visually distinct and easier to identify.
  • UNII YC9ST449YJ
    Ethyl vanillin is a synthetic vanilla flavoring compound. It's added to medicines to mask bitter or unpleasant tastes, making them easier to take.
  • 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 EX438O2MRT
    Ferric oxide yellow is a naturally occurring iron compound used as a colorant in medications. It gives tablets, capsules, and other forms a yellow or golden hue for identification and appearance.
  • UNII XM0M87F357
    A dark iron oxide compound that gives medicines their black or dark color. It's used as a colorant in tablets and capsules to help identify the product and make it visually distinctive.
  • 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 4PC054V79P
    A fatty acid derived from glycerin and oleic acid (a natural oil component). It acts as an emulsifier to help mix oil and water-based ingredients, and serves as a lubricant and surfactant in the formulation.
  • 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 YSE9PPT4TH
    Hyaluronate sodium is a natural carbohydrate that holds moisture. It's used in medicines as a lubricant, thickener, and moisture-retaining agent to improve texture and delivery of the active ingredient.
  • 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 461N1O614Y
    A synthetic oily liquid used as an emollient and solvent in medications. It helps dissolve active ingredients and improves how the medicine spreads or absorbs through the skin.
  • 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 CLV24I3T1D
    A plant extract from pomegranate root bark used as a natural coloring agent and flavoring component in medicines. It may also help preserve the product and provide mild astringent properties to the formulation.
  • 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 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 AZQ08K38Z1
    A synthetic oily liquid derived from salicylic acid. It works as an emollient and penetration enhancer in topical formulations, helping active ingredients absorb into skin while conditioning and softening the application area.
  • 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 231473QB6R
    Watermelon is a fruit extract or flavoring agent. It's added to medicines to improve taste, making the product more palatable, especially for children or medications with unpleasant flavors.
  • UNII 2ZA36H0S2V
    Beeswax is a natural wax produced by honeybees. In medicines, it works as a coating agent and thickener to control how fast the drug dissolves and improve the product's texture and appearance.

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

The official label also statesAloe Barbadensis Leaf Extract, Beeswax, Butyloctyl Salicylate, Camellia Sinensis Leaf Extract, Caprylic/Capric Triglyceride, Citrullus Lanatus (Watermelon) Fruit Extract, Ethyl Vanillin, Flavor (Aroma), Glycerin, Glyceryl Oleate, Helianthus Annuus (Sunflower) Seed Oil, Hydrogenated Polyisobutene, Iron Oxides (CI 77491), Iron Oxides (CI 77492), Iron Oxides (CI 77499), Octyldodecanol, Petrolatum, Punica Granatum Extract, Red 30 Lake (CI 73360), Ricinus Communis (Castor) Seed Oil, Sodium Hyaluronate, Stevia Rebaudiana Extract, Tocopherol, Tridecyl Salicylate, Water (Aqua)

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
Proven Personalized Day Moisturizer With SPF 50 150 mg/mL 73572-0004-30 Proven 30 ml — — FDA listed —
MIAMI BEACH BUM Save Face SPF-30 Sunscreen 150 mg/mL 82812-0336-00 MIAMI 100 ml — — FDA listed —
MIAMI BEACH BUM Blocked SPF-30 Sunscreen 150 mg/mL 82812-0337-00 MIAMI 180 ml — — FDA listed —
Slip Tint Broad Spectrum SPF 35 Tinted Moisturizer 150 mg/mL 90086-0012-01 Clean 40 ml — — FDA listed —
SEAWEED BATH CO Everyday Mineral SPF 40 150 mg/mL 81159-0259-00 The 100 ml — — FDA listed —
Miami Beach Bum SPF 30 Bodyguard Face Body Mineral Sunscreen 150 mg/mL 82812-0958-00 Miami 100 ml — — FDA listed —
Slip Tint Broad Spectrum SPF 35 Sunscreen Tinted Moisturizer Shade Four 150 mg/mL 90086-0017-01 Clean 1 tube — — FDA listed —
Sqween Paint-On Sun Protection for Independent Kids Mineral Sunscreen SPF 30 150 mg/mL 83005-0002-01 Sqween 118 ml — — FDA listed —
ETADERM Tattoo Sunscreen Broad Spectrum SPF-30 150 mg/mL 84180-0472-00 NUEPHASE 118 ml — — FDA listed —
Oathology Inzincable Lip Balm SPF 35 150 mg/mLthis 85562-0694-00 SKINOATH 1 tube — — FDA listed —
Slip Tint Broad Spectrum SPF 35 Sunscreen Tinted Moisturizer Shade Three and Half 150 mg/mL 90086-0016-01 Clean 1 tube — — FDA listed —
Slip Tint Broad Spectrum SPF 35 Sunscreen Tinted Moisturizer Shade Five 150 mg/mL 90086-0019-01 Clean 1 tube — — FDA listed —
Sun Bum Daily Mineral Sunscreen Moisturizer Broad Spectrum SPF 30 150 mg/mL 69039-0761-02 Sun 1 bottle — — FDA listed —
Saie Sunvisor Broad Spectrum SPF 35 Sheer Moisturizer 150 mg/mL 90086-0011-01 Clean 1 tube — — FDA listed —
Slip Tint Broad Spectrum SPF 35 Sunscreen Tinted Moisturizer Shade Four and Half 150 mg/mL 90086-0018-01 Clean 1 tube — — FDA listed —
Calendula Essential Hydrating Broad Spectrum SPF 30 Sunscreen 150 mg/mL 64657-0007-02 Naturopathica 1 tube — — FDA listed —
Slip Tint Broad Spectrum SPF 35 Sunscreen Tinted Moisturizer Shade Three 150 mg/mL 90086-0015-01 Clean 1 tube — — FDA listed —
Slip Tint Broad Spectrum SPF 35 Sunscreen Tinted Moisturizer Shade Nine 150 mg/mL 90086-0024-01 Clean 1 tube — — FDA listed —
Sqween 100% Mineral Sunscreen Broad Spectrum SPF 30 Water Resistant 150 mg/mL 83005-0001-01 SQWEEN 60 ml — — FDA listed —
Good Weather Skin The One Daily Sun Warm Glow SPF 30 150 mg/mL 85090-0002-01 Good 1 bottle — — FDA listed —
Slip Tint Broad Spectrum SPF 35 Sunscreen Tinted Moisturizer Shade Nine and Half 150 mg/mL 90086-0025-01 Clean 1 tube — — FDA listed —
Lion Pose Ghost-Buster Broad Spectrum Spf 42 Sunscreen 150 mg/mL 83605-0001-01 Lion 2 ml — — Discontinued —
Cancer Council Mineral Fluid SPF50 150 mg/mL 84258-0006-01 Vitality 1 tube — — FDA listed —
Slip Tint Broad Spectrum SPF 35 Sunscreen Tinted Moisturizer Shade One 150 mg/mL 90086-0013-01 Clean 1 tube — — FDA listed —
Slip Tint Broad Spectrum SPF 35 Sunscreen Tinted Moisturizer ShadeTwo 150 mg/mL 90086-0014-01 Clean 1 tube — — FDA listed —
Slip Tint Broad Spectrum SPF 35 Sunscreen Tinted Moisturizer Shade Eight 150 mg/mL 90086-0023-01 Clean 1 tube — — FDA listed —
Duke Cannon Supply Co. Daily Defense Face Mineral Sunscreen Broad Spectrum SPF 32 150 mg/mL 71782-0201-03 DUKE 1 tube — — FDA listed —
Slip Tint Broad Spectrum SPF 35 Sunscreen Tinted Moisturizer Shade Ten 150 mg/mL 90086-0026-01 Clean 1 tube — — FDA listed —
Slip Tint Broad Spectrum SPF 35 Sunscreen Tinted Moisturizer Shade Five and Half 150 mg/mL 90086-0020-01 Clean 1 tube — — FDA listed —
Slip Tint Broad Spectrum SPF 35 Sunscreen Tinted Moisturizer Shade Six 150 mg/mL 90086-0021-01 Clean 1 tube — — FDA listed —
Lion Pose Unghosted Tinted Mineral Spf 42 Uva Uvb Sunscreen 150 mg/mL 83605-0002-01 Lion 1 bottle — — FDA listed —
Slip Tint Broad Spectrum SPF 35 Sunscreen Tinted Moisturizer Shade Seven 150 mg/mL 90086-0022-01 Clean 1 tube — — FDA listed —
Sqween Mineral Sunscreen Broad Spectrum SPF 30 Light Green 150 mg/mL 83005-0005-01 Sqween 60 ml — — FDA listed —
Sqween Mineral Sunscreen Broad Spectrum SPF 30 Blue 150 mg/mL 83005-0003-01 Sqween 60 ml — — FDA listed —
Sqween Mineral Sunscreen Broad Spectrum SPF 30 Blue 150 mg/mL 58419-0011-00 Atlantis 60 ml — — FDA listed —
Sqween Mineral Sunscreen Broad Spectrum SPF 30 Pink 150 mg/mL 83005-0006-01 Sqween 60 ml — — FDA listed —
Sqween Mineral Sunscreen Broad Spectrum SPF 30 Gold 150 mg/mL 83005-0004-01 Sqween 60 ml — — FDA listed —
Sqween Mineral Sunscreen Broad Spectrum SPF 30 Rose Gold 150 mg/mL 83005-0007-01 Sqween 60 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

🏛️
2025
On the market since
Apr 2025
📍
2026
Currently FDA-listed
1 year 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
85562-0694-00 You're viewing this 1 TUBE in 1 BOX (85562-694-00) / 10 mL in 1 TUBE 2025-04-22 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 — Not published for this NDC No photo available yet for this listing.
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 85562-694-00, 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: 85562-0694-00, written without dashes as 85562069400. 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 85562-0694-00, the first segment (85562) is the labeler code FDA assigned to SKINOATH LLC; the middle segment (0694) identifies this specific product — its ingredient, strength, and dosage form; and the last segment (00) 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 SKINOATH LLC. Listing status can change — the directory data on this page refreshes weekly.
Who lists this product with the FDA?
SKINOATH 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 🧪 Active Ingredient 🧪 Inactive Ingredients 🎯 Purpose
🎯 Indications and Usage 35 words ▾

Uses: Helps prevent sunburn. Higher SPF gives more sunburn protection 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 93 words ▾

Directions: Apply liberally 15 minutes before sun exposure and as needed. 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 the risk, regularly use a sunscreen with 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.

⚠️ Warnings 68 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 or irritation develops and lasts. Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away. If pregnant or breast-feeding, ask a health professional before use

🧪 Active Ingredient 8 words ▾

Active Ingredients Zinc Oxide 15.00 % Purposes Sunscreen

🧪 Inactive Ingredients 71 words ▾

Inactive Ingredients: Aloe Barbadensis Leaf Extract, Beeswax, Butyloctyl Salicylate, Camellia Sinensis Leaf Extract, Caprylic/Capric Triglyceride, Citrullus Lanatus (Watermelon) Fruit Extract, Ethyl Vanillin, Flavor (Aroma), Glycerin, Glyceryl Oleate, Helianthus Annuus (Sunflower) Seed Oil, Hydrogenated Polyisobutene, Iron Oxides (CI 77491), Iron Oxides (CI 77492), Iron Oxides (CI 77499), Octyldodecanol, Petrolatum, Punica Granatum Extract, Red 30 Lake (CI 73360), Ricinus Communis (Castor) Seed Oil, Sodium Hyaluronate, Stevia Rebaudiana Extract, Tocopherol, Tridecyl Salicylate, Water (Aqua)

🎯 Purpose 2 words ▾

Purposes Sunscreen

Source: FDA Structured Product Labeling, mirrored from DailyMed / openFDA. Prefer the government’s original formatting? View this label on DailyMed ↗
← 85562-0594-00 · SKINOATH 85563-0202-50 · CLEAR →
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.