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Bliss Block Star Sheer Liquid Daily Sunscreen SPF 50 SPF-50 Zinc Oxide 20 g/100mL Lotion — NDC 67038-0203-60 package photo
Label image from the product's FDA listing (DailyMed) — may show a different pack size or an older label revision.

Bliss Block Star Sheer Liquid Daily Sunscreen SPF 50 SPF-50 Zinc Oxide 20 g/100mL Lotion — NDC 67038-203-60 (Billing 67038-0203-60)

by Bliss Products Holdings LLC · 1 BOTTLE, PLASTIC in 1 BOX / 60 mL in 1 BOTTLE, PLASTIC

This is a package of Bliss Block Star Sheer Liquid Daily Sunscreen SPF 50 SPF-50 Zinc Oxide 20 g/100mL Lotion from Bliss Products Holdings LLC, marketed since Jan 2023 and currently FDA-listed. It is this product's only package size.

NDC 67038-0203-60
🏷️ FDA NDC (as labeled) 67038-203-60 billing pads the product segment with a zero
OTC On market Non-controlled ⇄ Compare with another NDC
🗂️ FDA directory synced Oct 1, 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 67038-203-60 alone.

Record
FDA NDC Directory package listing · Human OTC drug
Code segments
67038 labeler · 203 product · 60 package
Package marketed since
Jan 31, 2023
Sample package
No — commercial package
Listing certified through
Dec 31, 2026
Barcode (UPC-A, from the NDC)
3 6703820360 6
FDA record last changed
Jul 24, 2026
⚠️
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

Regulatory identifiers FDA, NLM and CMS codes for this package

FDA NDC (as labeled) 67038-203-60
Product NDC 67038-203
11-digit billing NDC 67038020360
UNII SOI2LOH54Z
Application # M020
SPL Set ID f262e5a7-3c57-a6d8-e053-2995a90aacbc
DEA schedule Non-controlled
Marketing category OTC MONOGRAPH DRUG
Marketing status On market
FDA listing status Listed (active directory)
Marketing start 2023-01-31
Route TOPICAL
Dosage form LOTION
Substance ZINC OXIDE
Why two NDCs? The FDA registers this code as 67038-203-60 — 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 → 67038-0203-60. 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 a topical lotion sunscreen containing zinc oxide, an inorganic UV filter commonly used in sun protection products. Zinc oxide is typically used to help protect skin from ultraviolet radiation by reflecting and scattering UV rays away from the skin. This product is marketed as an over-the-counter monograph drug, meaning it follows FDA's established safety and effectiveness standards for sunscreen ingredients rather than being individually reviewed. The lotion form is applied directly to exposed skin areas.

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.

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.

Packaging — all sizes for this product

Package NDCDescription Marketing startMarketing endStatus
67038-0203-60 You're viewing this Main listing 1 BOTTLE, PLASTIC in 1 BOX / 60 mL in 1 BOTTLE, PLASTIC 2023-01-31 — Active

Therapeutic equivalents

ProductLabelerPackNADAC/unitTEStatusPrice vs. this
Surface SPF 50 3oz Tinted mineral sunscreen with Water Resistance 20 g/100mL 72344-0112-03 Surface 88 ml — — FDA listed —
Solara Suncare - Clean Freak Spf-30 Naturally Scented 20 g/100mL 73054-0102-11 SOLARA 1 tube — — FDA listed —
Rio Radiance SPF 50 BodyLotion 20 g/100mL 83982-4838-00 SOL 1 tube — — FDA listed —
Thrive Daily Sunscreen For Sensitive Skin SPF 30 20 g/100mL 84138-0002-02 Thrive 1 bottle — — FDA listed —
Spf-30 Bb 20 g/100mL 69090-0100-01 ZION 110 ml — — FDA listed —
Native Mineral Sunscreen Broad Spectrum SPF 30 Unscented 20 g/100mL 69423-0550-14 The 147 ml — — Discontinued —
Solara Suncare - Fortune Teller Spf-30 20 g/100mL 73054-0120-11 SOLARA 1 tube — — FDA listed —
Babyganics Kids Sheer Blend SPF50 Mineral Sunscreen 20 g/100mL 59062-2203-03 KAS 89 ml — — FDA listed —
Sunceutical SPF 50 Mineral Body Cream 20 g/100mL 70157-0368-02 Baxter 1 jar — — FDA listed —
SPF 50 Mineral Sunscreen Face and Body 20 g/100mL 85865-0002-01 Toddle 50 ml — — FDA listed —
BOA VIDA Calvida 20 g/100mL 62654-0145-04 Central 118 ml — — FDA listed —
Sheer Mineral Sunscreen 20 g/100mL 84009-0816-01 Plant 1 tube — — FDA listed —
Native Mineral Sunscreen Broad Spectrum SPF 30 Tropical Breeze 20 g/100mL 84126-0605-14 The 147 ml — — FDA listed —
Ava Isa Sun Lip Sun Whip Strawberry Zinnia 20 g/100mL 71644-0010-10 Cyberderm 1 tube — — FDA listed —
Solara Suncare - Glow Getter Spf-30 Naturally Scented 20 g/100mL 73054-0103-11 SOLARA 1 tube — — FDA listed —
Solara Suncare - Time Traveler Spf-30 Unscented 20 g/100mL 73054-0105-11 SOLARA 1 tube — — FDA listed —
Native Mineral Suncare Daily Face Broad Spectrum SPF 30 Unscented 20 g/100mL 84126-0157-50 The 1 tube — — FDA listed —
Thrive Daily Defense Sunscreen Balm SPF30 20 g/100mL 84138-0001-02 Thrive 1 bottle — — FDA listed —
Surface Sun SPF 50 Mineral 20 g/100mL 72344-0110-03 Surface 88 ml — — FDA listed —
ARAMORE MULTI-DEFENSE SUNSCREEN - AM Broad Spectrum SPF 30 20 g/100mL 83127-0101-11 New 50 ml — — FDA listed —
Native Mineral Suncare Broad Spectrum SPF 30 Unscented 20 g/100mL 84126-0156-14 The 147 ml — — FDA listed —
Babyganics Sheer Blend SPF50 Mineral Sunscreen 20 g/100mL 59062-2202-01 KAS 50 ml — — FDA listed —
Native Mineral Face Broad Spectrum SPF 30 Unscented 20 g/100mL 69423-0548-50 The 50 ml — — Discontinued —
Native Facial Care Brightening Facial Moisturizer Broad Spectrum SPF 30 20 g/100mL 69423-0621-50 The 1 bottle — — FDA listed —
Native Mineral Sunscreen Broad Spectrum SPF 30 Sweet Peach and Nectar 20 g/100mL 69423-0731-14 The 147 ml — — FDA listed —
Sunceutical SPF 50 Mineral Glow Serum 20 g/100mL 70157-0367-02 Baxter 1 jar — — FDA listed —
Sunceutical SPF 50 Mineral Face Cream 20 g/100mL 70157-0369-02 Baxter 1 jar — — FDA listed —
Ava Isa Sun Lip Sun Whip Clear Sunshine 20 g/100mL 71644-0009-10 Cyberderm 1 tube — — FDA listed —
Mineral Defense Sport Antioxidant Face Sunscreen Spf-50 20 g/100mL 73054-0107-11 SOLARA 1 tube — — FDA listed —
Silk Mineral SPF 50 Sunscreen Face 20 g/100mL 70157-0026-01 Baxter 50 ml — — FDA listed —
Ava Isa Sun Lip Sun Whip Watermelon Lily 20 g/100mL 71644-0011-10 Cyberderm 1 tube — — FDA listed —
Native Daily Face Mineral Sunscreen Broad Spectrum SPF 30 Coconut and Pineapple 20 g/100mL 84126-0112-50 The 50 ml — — FDA listed —
Native Mineral Suncare Broad Spectrum SPF 30 Coconut and Pineapple 20 g/100mL 84126-0155-14 The 147 ml — — FDA listed —
Sol de Janiero Rio Radiance SPF 50 Body 20 g/100mL 66163-4838-01 Cosmetic 1 bottle — — FDA listed —
Native Mineral Face Broad Spectrum SPF 30 Coconut and Pineapple 20 g/100mL 69423-0549-50 The 50 ml — — Discontinued —
Solara Suncare - Clean Freak Spf-30 Unscented 20 g/100mL 73054-0101-11 SOLARA 1 tube — — FDA listed —
Bliss Block Star Sheer Liquid Daily Sunscreen SPF 50 SPF-50 20 g/100mLthis 67038-0203-60 Bliss 1 bottle — — FDA listed —
First Aid Beauty FAB Mineral Sunscreen Broad Spectrum SPF 30 20 g/100mL 69423-0622-50 The 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

🏛️
2023
On the market since
Jan 2023
📍
2026
Currently FDA-listed
3 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.

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 16AE65F94Y
    A natural aromatic compound derived from plant sources like chamomile oil. It's used as a fragrance agent and may help preserve the medicine's stability and scent during storage.
  • UNII DI775RT244
    A natural fatty acid derived from coconut or palm oil. Used as an emulsifier and solubilizer to help mix oil and water components and improve how the medicine dissolves and absorbs in the body.
  • UNII 2DMT128M1S
    A waxy solid derived from plant or animal sources. It acts as an emulsifier to blend oil and water components, and also thickens the medicine to give it the right texture and consistency.
  • UNII 5B8915UELW
    A plant-derived compound used as an antioxidant in medicines. It helps prevent spoilage and degradation of active ingredients during storage by protecting them from oxidative damage.
  • UNII WQ29KQ9POT
    Gluconolactone is a mild organic acid derived from glucose. It functions as a buffer and pH regulator in medicines, helping maintain stable acidity levels and improve product stability.
  • 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 86FQE96TZ4
    A synthetic polymer, this ingredient acts as a thickener and suspending agent in liquid formulations. It helps maintain uniform consistency and keeps particles evenly distributed throughout the medicine.
  • 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 4KDO9AFM9I
    A plant-derived emulsifier made from olive oil and polyglycerols. It helps mix oil and water-based ingredients together and improves the texture and stability of the medicine.
  • UNII X958PZJ9ON
    A synthetic emulsifier derived from sorbitol and polyethylene glycol. It helps mix oil and water-based ingredients together in liquid or semi-solid formulations, improving texture and consistency.
  • 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 CAL22UVI4M
    A synthetic emulsifier derived from sorbitol and fatty acids. It helps mix oil and water-based ingredients together and improves the texture and stability of the medicine.
  • UNII 6OZP39ZG8H
    Polysorbate 80 is a synthetic emulsifier derived from sorbitol and oleic acid. It helps mix oil and water-based ingredients together in medications and improves how the product disperses in the body.
  • UNII OJ245FE5EU
    Sodium benzoate is a salt derived from benzoic acid, a preservative. It's added to medicines to prevent growth of bacteria, fungi, and other microorganisms that could spoil the product.
  • UNII IN99IT31LN
    Sodium stearoyl lactylate is a synthetic compound made from stearic acid and lactic acid. It works as an emulsifier to help keep oils and water mixed together, and as a dough conditioner in solid dosage forms.
  • 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 5EHL50I4MY
    A sodium salt compound used as a chelating agent in medicines. It binds to metals and minerals to improve stability, prevent discoloration, and help the medication stay effective longer.
  • 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 KFR5QEN0N9
    A synthetic plastic polymer that helps form a protective film coating on the medicine. It's used as a binder and film-former to hold the tablet or capsule together and control how quickly the drug dissolves.
  • 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 TTV12P4NEE
    Xanthan gum is a thickening and stabilizing ingredient made from fermented corn or other sugars. It's added to medicines to improve texture, prevent separation of liquids and solids, and help the product stay consistent.

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

The official label also statesWater, Caprylic/Capric Triglyceride, Glycerin, VP/Hexadecene Copolymer, Dimethicone, Sorbitan Isostearate, Helianthus Annuus (Sunflower) Seed Oil, Bisabolol, Xanthan Gum, Cetearyl Alcohol, Ethyl Ferulate, Olive Oil Polyglyceryl-6 Esters, Hydroxyethyl Acrylate/Sodium Acryloyldimethyl Taurate Copolymer, Glyceryl Stearate, Polysorbate 60, Polysorbate 80, Sodium Stearoyl Lactylate, Triethoxycaprylylsilane, Isohexadecane, Gluconolactone, Tetrasodium Glutamate Diacetate, Phenoxyethanol, Sodium Benzoate

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

LabelerBliss Products Holdings LLC
FDA applicationM020 (OTC MONOGRAPH DRUG)
Labeler code67038
First marketedJan 2023
Product typeHuman Otc Drug
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 📦 Storage and Handling 🧪 Active Ingredient 🧪 Inactive Ingredients 🎯 Purpose 📄 Keep Out of Reach of Children 📄 Package Label / Principal Display Panel
🎯 Indications and Usage 30 words ▾

• 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 93 words ▾

• Apply liberally 15 minutes before sun exposure • Reapply: • after 80 minutes of swimming or sweating • immediately after towel drying • at least every 2 hours • 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 37 words ▾

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

📦 Storage and Handling 10 words ▾

• Protect this product from excessive heat and direct sun

🧪 Active Ingredient 3 words ▾

Zinc Oxide 20%

🧪 Inactive Ingredients 48 words ▾

Water, Caprylic/Capric Triglyceride, Glycerin, VP/Hexadecene Copolymer, Dimethicone, Sorbitan Isostearate, Helianthus Annuus (Sunflower) Seed Oil, Bisabolol, Xanthan Gum, Cetearyl Alcohol, Ethyl Ferulate, Olive Oil Polyglyceryl-6 Esters, Hydroxyethyl Acrylate/Sodium Acryloyldimethyl Taurate Copolymer, Glyceryl Stearate, Polysorbate 60, Polysorbate 80, Sodium Stearoyl Lactylate, Triethoxycaprylylsilane, Isohexadecane, Gluconolactone, Tetrasodium Glutamate Diacetate, Phenoxyethanol, Sodium Benzoate

🎯 Purpose 1 words ▾

Sunscreen

📄 Keep Out of Reach of Children 20 words ▾

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

📄 Package Label / Principal Display Panel 1 words ▾

Label

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

Reported adverse events (FAERS)

Read carefully: FAERS reports are voluntary and unverified. Counts are not incidence, do not establish causation, are subject to reporting bias, and cannot be used to compare one drug to another. Shown for signal context only. Reports for Bliss Block Star Sheer Liquid Daily Sunscreen SPF 50 SPF-50 (this brand).

Top reported reactions

Macular Degeneration460
Pyrexia306
Nausea290
Pain282
Malaise261
Weight Decreased236
Therapeutic Product Effect Incomplete214

Reporter sex

1,941 reports
Male · 37%
Female · 63%
Unknown · 0%

Serious outcomes

Life-threatening116
Disabling32
Reports over time (by year) — tap or hover for the count & year
2020 2022 2024 2026 272 0
Most recent year is provisional (FAERS lags ~3 months).
Where does this data come from?
Adverse-event reports from the FDA Adverse Event Reporting System (FAERS) via openFDA. FAERS reports are voluntary and unverified — counts are not incidence and don’t establish causation.

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 Bliss Products Holdings LLC. Listing status can change — the directory data on this page refreshes weekly.
Who lists this product with the FDA?
Bliss Products Holdings 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.
← 67015-2036-01 · Pierre 67046-0007-03 · Coupler →
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.