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HEB 50 Pumpkin Spice Latte Scent Sunscreen AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE 30 mg/g; 100 mg/g; 50 mg/g; 40 mg/g Spray, 156 g — NDC 37808-0940-37 package photo

HEB 50 Pumpkin Spice Latte Scent Sunscreen AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE 30 mg/g; 100 mg/g; 50 mg/g; 40 mg/g Spray, 156 g

by H.E.B. · 156 g in 1 CAN (37808-940-37)
NDC 37808-0940-37
🏷️ FDA NDC (as labeled) 37808-940-37 billing pads the product segment with a zero
OTC On market Non-controlled
🗂️ Data synced Sep 3, 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) 37808-940-37
Product NDC 37808-940
11-digit billing NDC 37808094037
UNII G63QQF2NOX, V06SV4M95S, 4X49Y0596W, 5A68WGF6WM
Application # M020
SPL Set ID 579f3274-398e-7eab-e063-6394a90afe35
DEA schedule Non-controlled
Marketing category OTC MONOGRAPH DRUG
Marketing status On market
FDA listing status Listed (active directory)
Marketing start 2026-09-01
Route TOPICAL
Dosage form SPRAY
Substance AVOBENZONE; HOMOSALATE; OCTISALATE; OCTOCRYLENE
Why two NDCs? The FDA registers this code as 37808-940-37 — 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 → 37808-0940-37. 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

LabelerH.E.B.
FDA applicationM020 (OTC MONOGRAPH DRUG)
Labeler code37808
First marketedSep 2026
Product typeHuman Otc Drug
Portfolio16 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?

This is an over-the-counter sunscreen spray marketed under the FDA's monograph rule for sunscreen products. It contains four UV-filtering ingredients (avobenzone, homosalate, octisalate, and octocrylene) that are typically used together to absorb ultraviolet radiation and help protect skin from sun exposure. The product is applied topically as a spray to exposed skin areas. Like all monograph sunscreens, it follows established FDA standards for this category of product.

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 JU3XHR8VWK
    A synthetic plastic polymer used as a film-coating agent. It forms a protective layer around tablets or capsules to control how and where the medicine dissolves in your digestive system.
  • UNII 3K9958V90M
    A liquid solvent derived from fermentation or chemical synthesis. In medicines, alcohol dissolves active ingredients, helps preserve the product, and improves how the body absorbs certain drugs.
  • UNII 3XUS85K0RA
    Butylene glycol is a clear liquid derived from petroleum or plants that acts as a humectant, solvent, and preservative booster in medicines. It helps keep formulations stable, dissolve active ingredients, and maintain moisture in topical products.
  • 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 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 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 WV9CM0O67Z
    Panthenol is a humectant and skin-conditioning agent derived from pantothenic acid. It's added to medicines to help retain moisture and soothe skin irritation.
  • UNII 2S713A4VP3
    A plant-derived resin from the podophyllum plant root. It acts as a binder and thickening agent to help hold tablet or capsule ingredients together and give the medicine its solid form.

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

The official label also statesacrylates/octylacrylamide copolymer, butylene glycol, butyloctyl salicylate, caprylic/capric triglyceride, fragrance, glycerin, panthenol, saccharomyces/podophyllum peltatum ferment filtrate, SD alcohol 40-B, tocopherol.

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 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.

🔁 Therapeutic equivalents

ProductLabelerPackNADAC/unitTEStatusPrice vs. this
Rite Aid Ryshi Sunscreen with Hyaluronic Acid and Collagen Broad Spectrum SPF 50 30 mg/g; 100 mg/g; 50 mg/g; 40 mg/g 11822-0027-01 Rite 156 g — — FDA listed —
HEB SPF 50 Rosewater Scented Continuous Sunscreen 30 mg/g; 100 mg/g; 50 mg/g; 40 mg/g 37808-0125-37 H.E.B 156 g — — FDA listed —
Aldi LACURA Sport Sunscreen 50 Broad Spectrum SPF 50 Continuous 30 mg/g; 100 mg/g; 50 mg/g; 40 mg/g 64024-0950-37 ALDI 156 g — — FDA listed —
Walgreens 50 Watermelon Scented Continuous Sunscreen 30 mg/g; 100 mg/g; 50 mg/g; 40 mg/g 00363-0387-37 WALGREEN 156 g — — FDA listed —
HEB SPF 50 Tattoo Continuous Sunscreen 30 mg/g; 100 mg/g; 50 mg/g; 40 mg/g 37808-0139-37 H.E.B 156 g — — FDA listed —
Wegmans Sport and Kids Clear Continuous Sunscreen 30 mg/g; 100 mg/g; 50 mg/g; 40 mg/g 47124-0126-37 WEGMANS 156 g — — FDA listed —
Aldi Lacura Kids Spf 50 Sunscreen 30 mg/g; 100 mg/g; 50 mg/g; 40 mg/g 64024-0944-37 ALDI 156 g — — FDA listed —
Berkley Jensen Sport Sunscreen SPF 50 30 mg/g; 100 mg/g; 50 mg/g; 40 mg/g 68391-0002-78 BJWC 2 cans — — FDA listed —
HEB SPF 50 White Gardenia Continuous Sunscreen 30 mg/g; 100 mg/g; 50 mg/g; 40 mg/g 37808-0083-37 H.E.B 156 g — — FDA listed —
HEB SPF 50 Cucumber Water Scented Continuous Sunscreen 30 mg/g; 100 mg/g; 50 mg/g; 40 mg/g 37808-0118-37 H.E.B 156 g — — FDA listed —
HEB SPF 50 Shine Sunscreen with Vitamin C Continuous Sunscreen 30 mg/g; 100 mg/g; 50 mg/g; 40 mg/g 37808-0193-37 H.E.B 156 g — — FDA listed —
Exchange Select Kids Spf 50 30 mg/g; 100 mg/g; 50 mg/g; 40 mg/g 55301-0021-37 Army 156 g — — FDA listed —
Walgreens 50 Banana Scented Continuous Sunscreen 30 mg/g; 100 mg/g; 50 mg/g; 40 mg/g 00363-0398-37 WALGREEN 156 g — — FDA listed —
Walgreens 50 Passion Fruit Scented Sunscreen 30 mg/g; 100 mg/g; 50 mg/g; 40 mg/g 00363-1360-37 WALGREEN 156 g — — FDA listed —
HEB SPF 50 Peach Bellini Scented Continuous Sunscreen 30 mg/g; 100 mg/g; 50 mg/g; 40 mg/g 37808-0108-37 H.E.B 156 g — — FDA listed —
HEB SPF 50 Refine 50 Sunscreen with Niacinamide and Collagen Continuous Sunscreen 30 mg/g; 100 mg/g; 50 mg/g; 40 mg/g 37808-0142-37 H.E.B 156 g — — FDA listed —
HEB SPF 50 Pink Peony Continuous Sunscreen 30 mg/g; 100 mg/g; 50 mg/g; 40 mg/g 37808-0086-37 H.E.B 156 g — — FDA listed —
HEB SPF 50 Rejuvenate Sunscreen with Moisturizing Oils and Vitamins Continuous Sunscreen 30 mg/g; 100 mg/g; 50 mg/g; 40 mg/g 37808-0189-37 H.E.B 156 g — — FDA listed —
Big Lots Soundbody Kids Sunscreen Spf 50 30 mg/g; 100 mg/g; 50 mg/g; 40 mg/g 50594-0152-37 BIG 156 g — — FDA listed —
Exchange Select Sport Sunscreen Continuous Spf 50 30 mg/g; 100 mg/g; 50 mg/g; 40 mg/g 55301-0042-63 Army 2 cans — — FDA listed —
Equate Sunscreen Spf 50 Sport Broad Spectrum 30 mg/g; 100 mg/g; 50 mg/g; 40 mg/g 79903-0398-18 Walmart 2 cans — — FDA listed —
HEB SPF 50 Hydrate 50 Sunscreen with Hyaluronic Acid and Collagen Continuous Sunscreen 30 mg/g; 100 mg/g; 50 mg/g; 40 mg/g 37808-0143-37 H.E.B 156 g — — FDA listed —
H-E-B Solutions Sunscreen Coconut Spf 50 Continuous 30 mg/g; 100 mg/g; 50 mg/g; 40 mg/g 37808-0905-37 H.E.B 156 g — — FDA listed —
Walgreens 50 Coconut Scented Continuous Sunscreen 30 mg/g; 100 mg/g; 50 mg/g; 40 mg/g 00363-0389-37 WALGREEN 156 g — — FDA listed —
HEB SPF 50 For Men Continuous Sunscreen 30 mg/g; 100 mg/g; 50 mg/g; 40 mg/g 37808-0078-37 H.E.B 156 g — — FDA listed —
HEB SPF 50 Watermelon Serbert Continuous Sunscreen 30 mg/g; 100 mg/g; 50 mg/g; 40 mg/g 37808-0089-37 H.E.B 156 g — — FDA listed —
HEB SPF 50 Mangonada Scented Continuous Sunscreen 30 mg/g; 100 mg/g; 50 mg/g; 40 mg/g 37808-0172-37 H.E.B 156 g — — FDA listed —
HEB SPF 50 Mexican Vanilla Scented Continuous Sunscreen 30 mg/g; 100 mg/g; 50 mg/g; 40 mg/g 37808-0185-37 H.E.B 156 g — — FDA listed —
Walgreens 50 Caramel and Pistachio Scented Sunscreen 30 mg/g; 100 mg/g; 50 mg/g; 40 mg/g 00363-1361-37 WALGREEN 156 g — — FDA listed —
Walgreens 50 Pina Colada Scented Sunscreen 30 mg/g; 100 mg/g; 50 mg/g; 40 mg/g 00363-4301-37 WALGREEN 156 g — — FDA listed —
Equaline Kids Spf 50 30 mg/g; 100 mg/g; 50 mg/g; 40 mg/g 41163-0953-37 United 156 g — — FDA listed —
HEB SPF 50 Pomegranate Continuous 30 mg/g; 100 mg/g; 50 mg/g; 40 mg/g 37808-0076-37 H.E.B 156 g — — FDA listed —
HEB SPF 50 Birthday Cake Continuous Sunscreen 30 mg/g; 100 mg/g; 50 mg/g; 40 mg/g 37808-0088-37 H.E.B 156 g — — FDA listed —
HEB SPF 50 Strawberry Daquiri Scented Continuous Sunscreen 30 mg/g; 100 mg/g; 50 mg/g; 40 mg/g 37808-0114-37 H.E.B 156 g — — FDA listed —
HEB SPF 50 Chamomile and Lavender Scented Continuous Sunscreen 30 mg/g; 100 mg/g; 50 mg/g; 40 mg/g 37808-0187-37 H.E.B 156 g — — FDA listed —
HEB 50 Marigold Scent Sunscreen 30 mg/g; 100 mg/g; 50 mg/g; 40 mg/g 37808-0899-37 H.E.B. 156 g — — FDA listed —
Sun Wave Anti Aging Insta Dry SPF 30 30 mg/g; 100 mg/g; 50 mg/g; 40 mg/g 84665-0000-00 Sun 155 g — — FDA listed —
HEB 50 Pumpkin Spice Latte Scent Sunscreen 30 mg/g; 100 mg/g; 50 mg/g; 40 mg/gthis 37808-0940-37 H.E.B. 156 g — — FDA listed —
Sun Wave Cross Sport Insta Dry SPF 30 30 mg/g; 100 mg/g; 50 mg/g; 40 mg/g 84665-0006-00 Sun 155 g — — FDA listed —
Walmart Equate Sunscreen Spf 50 Sport Broad Spectrum 30 mg/g; 100 mg/g; 50 mg/g; 40 mg/g 79903-0379-02 WALMART, 2 cans — — 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
Sep 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.

🔬 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
Life-threatening11
Reports over time (by year) — tap or hover for the count & year
2023 2024 2025 2026 52 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.

📦 Packaging — all sizes for this product

Package NDCDescription Marketing startStatus
37808-0940-37 You're viewing this 156 g in 1 CAN (37808-940-37) 2026-09-01 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 ✓ 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 37808-940-37, 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: 37808-0940-37, written without dashes as 37808094037. 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 37808-0940-37, the first segment (37808) is the labeler code FDA assigned to H.E.B.; the middle segment (0940) identifies this specific product — its ingredient, strength, and dosage form; and the last segment (37) 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 H.E.B.. Listing status can change — the directory data on this page refreshes weekly.
Who lists this product with the FDA?
H.E.B. 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 and Cautions ⚠️ Warnings 🧪 Active Ingredient 🧪 Inactive Ingredients 🎯 Purpose
🎯 Indications and Usage 30 words ▾

Uses helps prevent sunburn if used as directed with other sun protetion measures (see Directions ), decreases the risk of skin cancer and early skin aging caused by the sun

⏱️ Dosage and Administration 139 words ▾

Directions spray liberally and spread evenly by hand 15 minutes before sun exposure hold can 4-6 inches away from the skin to apply do not spray into face. Spray into hands then apply to face. do not apply in windy conditions use in a well-ventilated area 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 and Cautions 17 words ▾

Flammable: do not use near heat, flame or while smoking avoid long term stoage above 104°F (40°C)

⚠️ Warnings 5 words ▾

Warnings For external use only

🧪 Active Ingredient 10 words ▾

Active Ingredients Avobenzone 3%, Homosalate 10%, Octisalate 5%, Octocrylene 4%

🧪 Inactive Ingredients 21 words ▾

Inactive Ingredients acrylates/octylacrylamide copolymer, butylene glycol, butyloctyl salicylate, caprylic/capric triglyceride, fragrance, glycerin, panthenol, saccharomyces/podophyllum peltatum ferment filtrate, SD alcohol 40-B, tocopherol.

🎯 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 ↗
← 37808-0939-18 · H.E.B. 37808-0942-86 · H →
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.