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Wegmans Kids and Sport Broad Spectrum SPF 50 Sunscreen Avobenzone, Homosalate, Octisalate, Octocrylene 50 mg/mL; 50 mg/mL; 150 mg/mL; 30 mg/mL Lotion, 89 mL — NDC 47124-0125-09 package photo

Wegmans Kids and Sport Broad Spectrum SPF 50 Sunscreen Avobenzone, Homosalate, Octisalate, Octocrylene 50 mg/mL; 50 mg/mL; 150 mg/mL; 30 mg/mL Lotion, 89 mL

by WEGMANS FOOD MARKETS INC · 89 mL in 1 BOTTLE (47124-125-09)
NDC 47124-0125-09
🏷️ FDA NDC (as labeled) 47124-125-09 billing pads the product segment with a zero
This package
Contains89 mL Pack sizes3 compare ↓
Also comes in: 237 ml 47124-0125-11 473 ml 47124-0125-14
OTC On market Non-controlled
🗂️ Data synced Aug 27, 2026 · sources: openFDA · FDA label (DailyMed) · FDA Orange & Purple Book · First Databank · CMS NADAC, ASP, Medicare & Medicaid · RxNorm
📋 All sources & update times →

This page is curated, coded, and maintained by

Compiled from public FDA, CMS, DailyMed, NADAC, and related drug data sources. Editorial policy

🆔 Identity & classification

FDA NDC (as labeled) 47124-125-09
Product NDC 47124-125
11-digit billing NDC 47124012509
UNII 5A68WGF6WM, 4X49Y0596W, V06SV4M95S, G63QQF2NOX
Application # M020
SPL Set ID f3463f81-9a65-3796-e053-2995a90a4f80
DEA schedule Non-controlled
Marketing category OTC MONOGRAPH DRUG
Marketing status On market
FDA listing status Listed (active directory)
Marketing start 2019-01-16
Route TOPICAL
Dosage form LOTION
Substance OCTOCRYLENE; OCTISALATE; HOMOSALATE; AVOBENZONE
Why two NDCs? The FDA registers this code as 47124-125-09 — 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 → 47124-0125-09. 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

LabelerWEGMANS FOOD MARKETS INC
FDA applicationM020 (OTC MONOGRAPH DRUG)
Labeler code47124
First marketedJan 2019
Product typeHuman Otc Drug
Portfolio10 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?

Wegmans Kids and Sport Broad Spectrum SPF 50 is a topical lotion sunscreen marketed as an over-the-counter monograph product. It contains four UV-filtering ingredients (avobenzone, homosalate, octisalate, and octocrylene) that function as sun-protective agents typically used to help block ultraviolet radiation from the sun. This product is formulated as a broad-spectrum sunscreen, meaning it is designed to provide protection against both UVA and UVB rays.

Supplement & herbal interactions

🌿 Drug–supplement interaction checker →
Where does this data come from?
Plain-language summary from MedlinePlus (U.S. National Library of Medicine); supplement & herbal interactions and nutrient depletion data from the Natural Medicines database; our full guide is HelloPharmacist editorial content.

🧪 Inactive Ingredients / Excipients

Inactive ingredients, also called excipients, are components of the drug product other than the active ingredient. They may include fillers, dyes, coatings, preservatives, flavors, or other formulation ingredients.

💡 Tap an ingredient (hover on desktop) to see what it is and why it’s used.

  • UNII 7QWA1RIO01
    A synthetic form of vitamin E used as an antioxidant in medicines. It prevents oils and fats in the formulation from breaking down, helping the drug remain stable and effective during storage.
  • UNII LKG8494WBH
    Benzyl alcohol is a clear liquid used as a preservative and solvent in medicines. It helps prevent bacterial and fungal growth and dissolves other ingredients to create uniform liquid formulations.
  • UNII V5RS026Q0H
    A synthetic polymer made by combining several plastic-like compounds. It forms a protective coating on tablets or capsules to control where and when the medicine dissolves in the digestive system.
  • UNII 71DD5V995L
    A synthetic polymer derived from acrylic acid, crosslinked to form a gel-like substance. It thickens formulations, improves texture, and helps distribute active ingredients evenly in topical products like creams and gels.
  • UNII I670DAL4SZ
    A preservative that fights bacteria and fungi. It keeps medicines and topical products stable and safe from microbial contamination during storage and use.
  • UNII 7FLD91C86K
    Edetate disodium is a chemical compound that binds and removes certain metal ions. In medicines, it acts as a preservative and stabilizer by preventing metals like calcium from interfering with the product's shelf life and consistency.
  • UNII 5LKW3C543X
    A synthetic oily liquid derived from neopentyl glycol and heptanoic acid. It serves as an emollient and solvent in formulations, helping to dissolve or suspend active ingredients and improve the texture and spreadability of topical products.
  • UNII BQZ26235UC
    A synthetic ingredient made from ethylene oxide and oleyl alcohol. It acts as an emulsifier and surfactant to help mix oil and water-based ingredients together in the formulation.
  • UNII 77723GV81A
    A synthetic plastic polymer used as a film-forming agent and binder. It helps create a protective coating on tablets or capsules and improves how ingredients stick together in the formulation.
  • UNII 6DC9Q167V3
    Propylene glycol is a clear liquid derived from petroleum or vegetable sources. It acts as a solvent, humectant, and preservative in medicines, helping dissolve active ingredients and maintain product stability.
  • 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 9O3K93S3TK
    Trolamine is an alkaline compound used as a pH buffer and emulsifier in medicines. It helps neutralize acids, stabilize formulations, and enable mixing of oil and water-based ingredients.
  • 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.

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

The official label also stateswater, tridecyl salicylate, propylene glycol, styrene/acrylates copolymer, polyamide-8, neopentyl glycol diheptanoate, oleth-3, acrylates/C10-30 alkyl acrylate crosspolymer, triethanolamine, tocopherol, disodium EDTA, chlorphenesin, benzyl alcohol, fragrance

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.
Try another pack size: 237 ml 473 ml
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
CVS Health Sport SPF 50 Sunscreen 50 mg/mL; 50 mg/mL; 150 mg/mL; 30 mg/mL 51316-0030-11 CVS 237 ml — — FDA listed —
Fruit of the Earth LUV THAT SUN Kids Sunscreen Ultra SPF 50 50 mg/mL; 50 mg/mL; 150 mg/mL; 30 mg/mL 62217-0405-25 FRUIT 177 ml — — FDA listed —
Wegmans Kids and Sport Broad Spectrum SPF 50 Sunscreen 50 mg/mL; 50 mg/mL; 150 mg/mL; 30 mg/mLthis 47124-0125-09 WEGMANS 89 ml — — FDA listed —
Walgreens SPF 50 Hydrating 50 mg/mL; 50 mg/mL; 150 mg/mL; 30 mg/mL 00363-0136-09 WALGREEN 89 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

🏛️
2019
On the market since
Jan 2019
📍
2026
Currently FDA-listed
7 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.

📦 Packaging — all sizes for this product

Package NDCDescription Marketing startStatus
47124-0125-09 You're viewing this 89 mL in 1 BOTTLE (47124-125-09) 2019-01-16 Active
47124-0125-11 237 mL in 1 BOTTLE (47124-125-11) 2019-01-16 Active
47124-0125-14 473 mL in 1 BOTTLE (47124-125-14) 2019-01-16 Active

You're viewing the smallest of 3 pack sizes for this product.

Pack size FAQ

What quantity is in NDC 47124-0125-09?
NDC 47124-0125-09 contains 89 mL — 89 ml in 1 bottle.
What is the difference between NDC 47124-0125-09 and NDC 47124-0125-11?
Both are Wegmans Kids and Sport Broad Spectrum SPF 50 Sunscreen Avobenzone, Homosalate, Octisalate, Octocrylene 50 mg/mL; 50 mg/mL; 150 mg/mL; 30 mg/mL Lotion — the drug itself is identical. NDC 47124-0125-09 is the 89 mL package, while NDC 47124-0125-11 is the 237 ml package.
What NDC number is used to bill for this package of Wegmans Kids and Sport Broad Spectrum SPF 50 Sunscreen Avobenzone, Homosalate, Octisalate, Octocrylene 50 mg/mL; 50 mg/mL; 150 mg/mL; 30 mg/mL Lotion?
Bill NDC 47124-0125-09 — the 11-digit billing format is 47124012509. Pharmacy and medical claims use the 11-digit form; the FDA label may print a shorter form of the same code.

🧭 About this NDC listing & data coverage

Over-the-counter (OTC) product
What data is (and isn’t) available for this NDC — tap to expand
NDC identity (package / product / labeler codes) ✓ Available
Labeler ✓ Available
Product & package description ✓ Available
Marketing category & status ✓ Available
Active ingredient / dosage form / route ✓ Available
FDA label (SPL via DailyMed) ✓ Available
Package photos ✓ Available
Inactive ingredients (structured) ✓ Available
NADAC pharmacy acquisition price (CMS) — Not published for this NDC CMS publishes NADAC only for NDCs reported in its retail-pharmacy survey.
Orange Book / therapeutic-equivalence data — Not published for this NDC Applies only to products approved under an NDA/ANDA; many listings are out of scope.
HCPCS J-code billing crosswalk — Not published for this NDC Most self-administered / retail products have no J-code — that is normal.
Medicaid utilization (CMS SDUD) — Not published for this NDC CMS reports utilization only for NDCs with Medicaid claims above its privacy threshold.
“Not published” reflects what the public FDA / CMS / NLM sources provide for this exact package code — it is a property of the data feeds, not a judgment about the product.

Questions about this listing

Is this NDC FDA-approved?
An NDC listing does not by itself establish FDA approval — the NDC Directory records that a product is listed with FDA, not that it was reviewed and approved. This listing's marketing category is "Otc Monograph Drug". Products approved under an application carry an NDA, ANDA, or BLA number.
Why is there no price listed?
The pricing shown on our NDC pages comes from CMS NADAC, a voluntary survey of retail community pharmacy invoices. CMS does not publish a NADAC for every NDC — packages outside the retail survey (institutional and hospital products, bulk packages, discontinued items, and many OTC items) may never receive one. A missing price reflects the survey's scope, not this product's actual cost, and does not mean the product is free or unavailable.
Is the NDC printed on the package the same as the 11-digit billing NDC?
Yes, they identify this exact package in different formats. The FDA registers it as 47124-125-09, 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: 47124-0125-09, written without dashes as 47124012509. 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 47124-0125-09, the first segment (47124) is the labeler code FDA assigned to WEGMANS FOOD MARKETS INC; the middle segment (0125) identifies this specific product — its ingredient, strength, and dosage form; and the last segment (09) 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 WEGMANS FOOD MARKETS INC. Listing status can change — the directory data on this page refreshes weekly.
Does this product come in other package sizes?
Yes — the FDA directory lists 2 other package presentations of this same product, including 237 ml (47124-0125-11), 473 ml (47124-0125-14). Each has its own NDC and its own page — see the package list near the top of this page.
Who lists this product with the FDA?
WEGMANS FOOD MARKETS INC 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 📦 Storage and Handling 🧪 Active Ingredient 🧪 Inactive Ingredients 🎯 Purpose
🎯 Indications and Usage 31 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 102 words ▾

Directions • apply liberally 15 minutes before sun exposure reapply: • after 80 minutes of swimming or sweating • immediately after towel drying • at least every 2 hours • 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 5 words ▾

Warnings For external use only

📦 Storage and Handling 25 words ▾

Other information • protect the product in this container from excessive heat and direct sun • may stain or damage some fabrics, materials or surfaces

🧪 Active Ingredient 10 words ▾

Active ingredients Avobenzone 3.0%, Homosalate 15.0%, Octisalate 5.0%, Octocrylene 5.0%

🧪 Inactive Ingredients 26 words ▾

Inactive ingredients water, tridecyl salicylate, propylene glycol, styrene/acrylates copolymer, polyamide-8, neopentyl glycol diheptanoate, oleth-3, acrylates/C10-30 alkyl acrylate crosspolymer, triethanolamine, tocopherol, disodium EDTA, chlorphenesin, benzyl alcohol, fragrance

🎯 Purpose 2 words ▾

Purpose Sunscreen

Source: FDA Structured Product Labeling, mirrored from DailyMed / openFDA. Prefer the government’s original formatting? View this label on DailyMed ↗
← 47124-0124-09 · WEGMANS 47124-0126-37 · WEGMANS →
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.