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Baloom Panthenol Hydro Airy Sunscreen Avobenzone, Homosalate, Octisalate. Octocrylene 1.35 g/50g; 6.75 g/50g; 2.25 g/50g; 4.5 g/50g Lotion — NDC 87679-0010-03 package photo
Label image from the product's FDA listing (DailyMed) — may show a different pack size or an older label revision.

Baloom Panthenol Hydro Airy Sunscreen Avobenzone, Homosalate, Octisalate. Octocrylene 1.35 g/50g; 6.75 g/50g; 2.25 g/50g; 4.5 g/50g Lotion — NDC 87679-010-03 (Billing 87679-0010-03)

by ARSN KOREA · 4 BOX in 1 CARTON / 15 TUBE in 1 BOX / 50 g in 1 TUBE

This is a package of Baloom Panthenol Hydro Airy Sunscreen Avobenzone, Homosalate, Octisalate. Octocrylene 1.35 g/50g; 6.75 g/50g; 2.25 g/50g; 4.5 g/50g Lotion from ARSN KOREA, no longer marketed (first marketed May 2026), no longer in the FDA NDC Directory. It is this product's only package size.

NDC 87679-0010-03
🏷️ FDA NDC (as labeled) 87679-010-03 billing pads the product segment with a zero
OTC Discontinued Non-controlled ⚠ Discontinued by firm ⇄ Compare with another NDC
🗂️ FDA directory synced Oct 1, 2026 · this listing last changed Jul 14, 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

⚠️
Excluded from the active FDA NDC Directory. The labeler reported this product as discontinued, so it is excluded from the active NDC Directory. The listing was last certified through Sep 2026. A label may still appear on DailyMed, but the NDC is no longer in the current FDA NDC Directory. Search the FDA NDC Directory ↗

Identity & classification

Regulatory identifiers FDA, NLM and CMS codes for this package

FDA NDC (as labeled) 87679-010-03
Product NDC 87679-010
11-digit billing NDC 87679001003
UNII G63QQF2NOX, V06SV4M95S, 4X49Y0596W, 5A68WGF6WM
Application # M020
SPL Set ID 5148b638-f8a4-fa8b-e063-6294a90ac208
DEA schedule Non-controlled
Marketing category OTC MONOGRAPH DRUG
Marketing status Discontinued
FDA listing status Discontinued by firm (certified through Sep 2026)
Marketing start 2026-05-08
Route TOPICAL
Dosage form LOTION
Substance AVOBENZONE; HOMOSALATE; OCTISALATE; OCTOCRYLENE
Why two NDCs? The FDA registers this code as 87679-010-03 — 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 → 87679-0010-03. 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?

Baloom Panthenol Hydro Airy Sunscreen is a topical lotion marketed as an over-the-counter monograph sunscreen product. It contains four ultraviolet (UV) filter ingredients: avobenzone, homosalate, octisalate, and octocrylene, which are typically used together to protect skin from UVA and UVB radiation. The lotion also includes panthenol, commonly used in skin care products for its moisturizing properties. This product is formulated and sold under the FDA's established rules for over-the-counter sunscreen drugs rather than as an individually reviewed application.

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 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
87679-0010-03 You're viewing this Main listing 4 BOX in 1 CARTON / 15 TUBE in 1 BOX / 50 g in 1 TUBE 2026-05-08 — Discontinued by firm

Therapeutic equivalents

ProductLabelerPackNADAC/unitTEStatusPrice vs. this
Baloom Panthenol Hydro Airy Sunscreen 1.35 g/50g; 6.75 g/50g; 2.25 g/50g; 4.5 g/50gthis 87679-0010-03 ARSN 15 tubes — — Discontinued —
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
May 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.

From the label’s inactive-ingredient section1,2-Hexanediol, Ammonium Acryloyldimethyltaurate/VP Copolymer, Butyloctyl Salicylate, C20-22 Alcohols, C20-22 Alkyl Phosphate, Caprylyl Methicone, Centella Asiatica Extract, Cetyl Alcohol, Diethylhexyl 2,6-Naphthalate, Dipropylene Glycol, Ethylhexylglycerin, Fragrance, Glyceryl Stearate, Methyl Methacrylate Crosspolymer, Panthenol, Pentylene Glycol, Polyacrylate Crosspolymer-6, Silica, Tocopherol, Tromethamine, VP/Eicosene Copolymer, Water

This is label-wide narrative text, not a normalized exact-product ingredient list. A label can cover multiple strengths or packages.

Where does this data come from?
Source: official FDA Structured Product Labeling (SPL) via DailyMed and the openFDA label index. Structured IACT rows and label-wide narrative are kept separate; availability and product-level specificity depend on the submitted label.

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

LabelerARSN KOREA
FDA applicationM020 (OTC MONOGRAPH DRUG)
Labeler code87679
First marketedMay 2026
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.

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 📄 Do Not Use 📄 Ask a Doctor Before Use If 📄 When Using This Product 📄 Keep Out of Reach of Children 📄 Other Information 📄 Recent Major Changes 📄 Package Label / Principal Display Panel
🎯 Indications and Usage 11 words ▾

Indications & usage Indications & usage Indications & usage-Helps prevent sunburn

⏱️ Dosage and Administration 19 words ▾

Dosage & administration Dosage & administration -Apply liberally 15 minutes before sun exposure. Reapply at least every two hours

⚠️ Warnings 5 words ▾

Warning Warning-For external use only

🧪 Active Ingredient 18 words ▾

Active Ingredient Active Ingredient Avobenzone 2.7% ---------------------------------------------------- Sunscreen Homosalate 13.5% --------------------------------------------------- Sunscreen Octisalate 4.5% ------------------------------------------------------- Sunscreen Octocrylene 9.0%------------------------------------------------------Sunscreen

🧪 Inactive Ingredients 42 words ▾

Inactive Ingredients 1,2-Hexanediol, Ammonium Acryloyldimethyltaurate/VP Copolymer, Butyloctyl Salicylate, C20-22 Alcohols, C20-22 Alkyl Phosphate, Caprylyl Methicone, Centella Asiatica Extract, Cetyl Alcohol, Diethylhexyl 2,6-Naphthalate, Dipropylene Glycol, Ethylhexylglycerin, Fragrance, Glyceryl Stearate, Methyl Methacrylate Crosspolymer, Panthenol, Pentylene Glycol, Polyacrylate Crosspolymer-6, Silica, Tocopherol, Tromethamine, VP/Eicosene Copolymer, Water

🎯 Purpose 5 words ▾

Purpose Purpose-Sunscreen, Uses-Helps prevent sunburn

📄 Do Not Use 12 words ▾

Do not use Do not use on damaged skin, on broken skin

📄 Ask a Doctor Before Use If 20 words ▾

Ask a doctor to use for children under 6 months Ask a doctor to use for children under 6 months

📄 When Using This Product 21 words ▾

When using this product, When using this product, When using this product, keep out of eyes. Rinse with water to remove

📄 Keep Out of Reach of Children 27 words ▾

Keep Out Of Reach of Children Keep Out Of Reach of Children- If product is swallowed, get medical help or contact a Poison Control Center right away

📄 Other Information 15 words ▾

Other Safety Information Protect the product in this container from excessive heat and direct sun

📄 Recent Major Changes 6 words ▾

Dosage & administration Dosage & administration

📄 Package Label / Principal Display Panel 18 words ▾

Package Label Principal Display Panel Baloom 2% Panthenol Hydro Airy Sunscreen Broad Spectrum SPF 50. 1.69 fl.oz/50mL 1

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 Avobenzone, Homosalate, Octisalate. Octocrylene — the ingredient across all brands.

Top reported reactions

Rash40
Skin Cancer39
Pruritus31
Erythema26
Pain26
Dyspnoea25
Fatigue25

Age at onset

Infant1
Child6
Adolescent4
Adult61
Elderly45

Reporter sex

650 reports
Male · 36%
Female · 64%

Serious outcomes

Hospitalization99
Disabling23
Life-threatening11
Reports over time (by year) — tap or hover for the count & year
2022 2023 2024 2026 57 7
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 No longer marketed (per FDA listing data)
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.
What does the discontinued status mean for this NDC?
The labeler reported a marketing end date (or the listing was delisted), so this specific package is no longer actively marketed. Remaining stock may still be dispensed for a time, and the NDC stays valid for historical records and claims — but data feeds (pricing, labeling) typically stop updating for it. Other package sizes or other manufacturers' versions of the same medication may still be marketed — see the equivalents section where available.
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.
Who lists this product with the FDA?
ARSN KOREA 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.
← 87676-0001-01 · Babylist, 87679-0020-01 · ARSN →
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.