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JAFRA ALWAYS LONG WEAR FOUNDATION BROAD SPECTRUM SPF 15 SUNSCREEN 121 Homosalate,Octisalate,Zinc Oxide 4.25 g/100g; 4.75 g/100g; 6.75 g/100g Liquid — NDC 68828-0301-01 package photo
Label image from the product's FDA listing (DailyMed) — may show a different pack size or an older label revision.

JAFRA ALWAYS LONG WEAR FOUNDATION BROAD SPECTRUM SPF 15 SUNSCREEN 121 Homosalate,Octisalate,Zinc Oxide 4.25 g/100g; 4.75 g/100g; 6.75 g/100g Liquid — NDC 68828-301-01 (Billing 68828-0301-01)

by Distribuidora Comercial Jafra, S.A. de C.V. · 1 TUBE in 1 CARTON / 30 g in 1 TUBE

This is a package of JAFRA ALWAYS LONG WEAR FOUNDATION BROAD SPECTRUM SPF 15 SUNSCREEN 121 Homosalate,Octisalate,Zinc Oxide 4.25 g/100g; 4.75 g/100g; 6.75 g/100g Liquid from Distribuidora Comercial Jafra, S.A. de C.V., marketed since Feb 2026 and currently FDA-listed. It is this product's only package size.

NDC 68828-0301-01
🏷️ FDA NDC (as labeled) 68828-301-01 billing pads the product segment with a zero
OTC On market Non-controlled ⇄ Compare with another NDC
🗂️ FDA directory synced Oct 8, 2026 · this listing last changed 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

NDC database record

One package, one record: these facts belong to NDC 68828-301-01 alone.

Record
FDA NDC Directory package listing · Human OTC drug
Code segments
68828 labeler · 301 product · 01 package
Package marketed since
Feb 1, 2026
Sample package
No — commercial package
Listing certified through
Dec 31, 2027
Barcode (UPC-A, from the NDC)
3 6882830101 4
FDA record last changed
Jul 24, 2026

Identity & classification

Regulatory identifiers FDA, NLM and CMS codes for this package

FDA NDC (as labeled) 68828-301-01
Product NDC 68828-301
11-digit billing NDC 68828030101
UNII V06SV4M95S, 4X49Y0596W, SOI2LOH54Z
Application # M020
SPL Set ID 2dd51960-515f-4502-b261-5e5d5f57e091
DEA schedule Non-controlled
Marketing category OTC MONOGRAPH DRUG
Marketing status On market
FDA listing status Listed (active directory)
Marketing start 2026-02-01
Route TOPICAL
Dosage form LIQUID
Substance HOMOSALATE; OCTISALATE; ZINC OXIDE
Why two NDCs? The FDA registers this code as 68828-301-01 — 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 → 68828-0301-01. 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.

Clinical

🧪 What is this product?

This is an over-the-counter monograph sunscreen foundation sold as a liquid applied to the skin. It contains three active ingredients that function as ultraviolet light filters: homosalate and octisalate are organic compounds that absorb UV radiation, while zinc oxide is a mineral that reflects and scatters UV rays. The product is formulated to provide broad-spectrum sun protection rated SPF 15 and is intended for use as a cosmetic foundation with sun-protective properties.

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.

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 mLPer 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.

Packaging — all sizes for this product

Package NDCDescription Marketing startMarketing endStatus
68828-0301-01 You're viewing this Main listing 1 TUBE in 1 CARTON / 30 g in 1 TUBE 2026-02-01 — Active

Therapeutic equivalents

ProductLabelerPackNADAC/unitTEStatusPrice vs. this
Jafra Always Long Wear Foundation Broad Spectrum Spf 15 Sunscreen 212 4.25 g/100g; 4.75 g/100g; 6.75 g/100g 68828-0304-01 Distribuidora 1 packet — — FDA listed —
Jafra Always Long Wear Foundation Broad Spectrum Spf 15 Sunscreen 151 4.25 g/100g; 4.75 g/100g; 6.75 g/100g 68828-0316-01 Distribuidora 1 tube — — FDA listed —
Jafra Always Long Wear Foundation Broad Spectrum Spf 15 Sunscreen 421 4.25 g/100g; 4.75 g/100g; 6.75 g/100g 68828-0325-01 Distribuidora 1 tube — — FDA listed —
Jafra Always Long Wear Foundation Broad Spectrum Spf 15 Sunscreen 342 4.25 g/100g; 4.75 g/100g; 6.75 g/100g 68828-0323-01 Distribuidora 1 tube — — FDA listed —
Jafra Always Long Wear Foundation Broad Spectrum Spf 15 Sunscreen 110 4.25 g/100g; 4.75 g/100g; 6.75 g/100g 68828-0300-01 Distribuidora 1 tube — — FDA listed —
Jafra Always Long Wear Foundation Broad Spectrum Spf 15 Sunscreen 132 4.25 g/100g; 4.75 g/100g; 6.75 g/100g 68828-0302-01 Distribuidora 1 packet — — FDA listed —
Jafra Always Long Wear Foundation Broad Spectrum Spf 15 Sunscreen 232 4.25 g/100g; 4.75 g/100g; 6.75 g/100g 68828-0317-01 Distribuidora 1 tube — — FDA listed —
Jafra Always Long Wear Foundation Broad Spectrum Spf 15 Sunscreen 442 4.25 g/100g; 4.75 g/100g; 6.75 g/100g 68828-0327-01 Distribuidora 1 tube — — FDA listed —
Jafra Always Long Wear Foundation Broad Spectrum Spf 15 Sunscreen 250 4.25 g/100g; 4.75 g/100g; 6.75 g/100g 68828-0319-01 Distribuidora 1 tube — — FDA listed —
Jafra Always Long Wear Foundation Broad Spectrum Spf 15 Sunscreen 351 4.25 g/100g; 4.75 g/100g; 6.75 g/100g 68828-0324-01 Distribuidora 1 tube — — FDA listed —
Jafra Always Long Wear Foundation Broad Spectrum Spf 15 Sunscreen 430 4.25 g/100g; 4.75 g/100g; 6.75 g/100g 68828-0326-01 Distribuidora 1 tube — — FDA listed —
Jafra Always Long Wear Foundation Broad Spectrum Spf 15 Sunscreen 221 4.25 g/100g; 4.75 g/100g; 6.75 g/100g 68828-0315-01 Distribuidora 1 tube — — FDA listed —
Jafra Always Long Wear Foundation Broad Spectrum Spf 15 Sunscreen 331 4.25 g/100g; 4.75 g/100g; 6.75 g/100g 68828-0322-01 Distribuidora 1 tube — — FDA listed —
Jafra Always Long Wear Foundation Broad Spectrum Spf 15 Sunscreen 140 4.25 g/100g; 4.75 g/100g; 6.75 g/100g 68828-0303-01 Distribuidora 1 tube — — FDA listed —
Jafra Always Long Wear Foundation Broad Spectrum Spf 15 Sunscreen 241 4.25 g/100g; 4.75 g/100g; 6.75 g/100g 68828-0318-01 Distribuidora 1 tube — — FDA listed —
Jafra Always Long Wear Foundation Broad Spectrum Spf 15 Sunscreen 121 4.25 g/100g; 4.75 g/100g; 6.75 g/100gthis 68828-0301-01 Distribuidora 1 tube — — FDA listed —
Jafra Always Long Wear Foundation Broad Spectrum Spf 15 Sunscreen 320 4.25 g/100g; 4.75 g/100g; 6.75 g/100g 68828-0320-01 Distribuidora 1 packet — — 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
Feb 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.

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 A9EJ3J61HQ
    A synthetic liquid derived from benzoic acid and long-chain alcohols. It functions as a solvent and penetration enhancer in topical formulations, helping active ingredients dissolve and absorb into the skin.
  • UNII E4F12ROE70
    A refined mineral oil derived from crude petroleum containing 13 to 14 carbon chains. It acts as a solvent, emollient, and carrier in topical formulations to help dissolve active ingredients and improve product texture and spreadability.
  • UNII UF7620L1W6
    A synthetic silicone polymer that acts as a thickener and absorbent in medicines. It helps create the right texture, improves how the product feels on skin or in the mouth, and can absorb excess moisture or oil in formulations.
  • UNII 92RU3N3Y1O
    Dimethicone is a silicone-based oil that acts as an anti-foaming agent and lubricant in medicines. It reduces gas bubbles in liquid formulations and helps coat and protect the stomach lining when ingested.
  • UNII X687XDK09L
    A clay mineral processed to carry positive charges, used as a thickener and suspending agent in liquid medicines. It helps keep solid particles evenly distributed throughout the product.
  • 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 8TE0BZU36S
    A silicone-based compound that acts as an emulsifier and skin protectant in topical formulations. It helps blend oil and water ingredients together and creates a smooth, protective barrier on the skin's surface.
  • UNII A8289P68Y2
    Isododecane is a lightweight liquid hydrocarbon used as a solvent and spreadability agent in topical formulations. It helps dissolve active ingredients and makes the product easier to apply and absorb into the skin.
  • UNII 6777U11MKT
    A silicone-based lubricant and anti-foaming agent used to reduce surface tension and prevent foam formation during manufacturing and storage of the medication.
  • 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 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 8D08K3S51E
    Propylene carbonate is a clear liquid solvent derived from propylene. It helps dissolve or suspend active ingredients in liquid medicines and can improve how well the product flows and mixes.
  • UNII EU2PSP0G0W
    Silica dimethyl silylate is a silicon-based powder that acts as a glidant and anti-caking agent. It reduces friction between particles and helps powders flow smoothly during manufacturing and tablet compression.
  • 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 451W47IQ8X
    Sodium chloride is common table salt. It's used in medicines as a buffer to maintain proper pH, as a filler to add bulk, or to adjust the osmotic balance in liquid formulations.
  • UNII 1DI56QDM62
    A natural fatty substance from soybeans that helps mix oil and water-based ingredients together. It acts as an emulsifier and lubricant in medicines to improve texture and help the product break down properly in your body.
  • 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 LDC331P08E
    A silicone-based compound that acts as a glidant and flow agent in solid medications. It reduces friction between powder particles, helping the medicine flow smoothly during manufacturing and tablet compression.
  • UNII 5041RX63GN
    A synthetic silicon-based polymer used as a glidant and anti-caking agent. It helps powder particles flow smoothly and prevents clumping during manufacturing and storage.
  • 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.

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

The official label also statesWater, Isododecane, Trimethylsiloxysilicate, Petroleum Distillates, Hydroxypropylcocoate PEG-8 Dimethicone, Lecithin, Disteardimonium Hectorite, C12-15 Alkyl Benzoate, Silica, Glycerin, Sodium Chloride, Niacinamide, Dimethicone, Phenoxyethanol, Propylene Carbonate, Triethoxycaprylylsilane, Dimethicone Crosspolymer, Silica Dimethyl Silylate, Methicone, Titanium Dioxide/CI 77891, Iron Oxides/CI 77491/CI 77492/CI 77499

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.

Manufacturer & labeler

LabelerDistribuidora Comercial Jafra, S.A. de C.V.
FDA applicationM020 (OTC MONOGRAPH DRUG)
Labeler code68828
First marketedFeb 2026
Product typeHuman Otc Drug
Portfolio75 products on file

More NDCs from Distribuidora Comercial Jafra, S.A. de C.V. labeler code 68828

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.

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 📄 Package Label / Principal Display Panel
🎯 Indications and Usage 30 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

⏱️ Dosage and Administration 100 words ▾

Directions shake well before use apply liberally and evenly 15 minutes before sun exposure reapply at least every 2 hours use a water resistant sunscreen if swimming or sweating children under 6 months of age: Ask a doctor 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 55 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.

🧪 Active Ingredient 13 words ▾

Active ingredients Purpose Homosalate 4.25% Sunscreen Octisalate 4.75% Sunscreen Zinc Oxide 6.75% Sunscreen

🧪 Inactive Ingredients 40 words ▾

Inactive ingredients Water, Isododecane, Trimethylsiloxysilicate, Petroleum Distillates, Hydroxypropylcocoate PEG-8 Dimethicone, Lecithin, Disteardimonium Hectorite, C12-15 Alkyl Benzoate, Silica, Glycerin, Sodium Chloride, Niacinamide, Dimethicone, Phenoxyethanol, Propylene Carbonate, Triethoxycaprylylsilane, Dimethicone Crosspolymer, Silica Dimethyl Silylate, Methicone, Titanium Dioxide/CI 77891, Iron Oxides/CI 77491/CI 77492/CI 77499

📄 Package Label / Principal Display Panel 4 words ▾

image description image description

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

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 form printed on the packaging and shown on DailyMed is the one the FDA registered. Insurance claims use a fixed 11-digit 5-4-2 format, so the short segment is padded with a leading zero and the dashes are dropped. The Identity section at the top of this page lists each form of this code.
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 Distribuidora Comercial Jafra, S.A. de C.V.. Listing status can change — the directory data on this page refreshes weekly.
Who lists this product with the FDA?
Distribuidora Comercial Jafra, S.A. de C.V. 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.
← 68828-0300-01 · Distribuidora 68828-0302-01 · Distribuidora →
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.