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Bath and Body Works SPF Waikiki Beach Coconut Avobenzone,Homosalate,Octisalate,Octocrylene 10 mg/100mg; 3 mg/100mg; 10 mg/100mg; 5 mg/100mg Spray, 117 mg — NDC 62670-6689-00 package photo
Label image from the product's FDA listing (DailyMed) — may show a different pack size or an older label revision.

Bath and Body Works SPF Waikiki Beach Coconut Avobenzone,Homosalate,Octisalate,Octocrylene 10 mg/100mg; 3 mg/100mg; 10 mg/100mg; 5 mg/100mg Spray, 117 mg — NDC 62670-6689-0 (Billing 62670-6689-00)

by Bath & Body Works, Inc. · 117 mg in 1 CAN

This is a package of 117 mg of Bath and Body Works SPF Waikiki Beach Coconut Avobenzone,Homosalate,Octisalate,Octocrylene 10 mg/100mg; 3 mg/100mg; 10 mg/100mg; 5 mg/100mg Spray from Bath & Body Works, Inc., marketed since Feb 2024 and currently FDA-listed. It is the main listing for this product, which comes in 2 package sizes.

NDC 62670-6689-00
🏷️ FDA NDC (as labeled) 62670-6689-0 billing pads the package segment with a zero
This package
Contains117 mg Pack sizes2 compare ↓
Main listing for product 62670-6689 · Also comes in: 53 mg 62670-6689-1
OTC On market Non-controlled ⇄ Compare with another NDC
🗂️ FDA directory synced Oct 1, 2026 · this listing last changed 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

NDC database record

One package, one record: these facts belong to NDC 62670-6689-0 alone.

Record
FDA NDC Directory package listing · Human OTC drug
Code segments
62670 labeler · 6689 product · 0 package
Package marketed since
Feb 12, 2024
Sample package
No — commercial package
Listing certified through
Dec 31, 2027
Barcode (UPC)
0637293029175
FDA record last changed
Aug 27, 2026

Identity & classification

Regulatory identifiers FDA, NLM and CMS codes for this package

FDA NDC (as labeled) 62670-6689-0
Product NDC 62670-6689
11-digit billing NDC 62670668900
UNII 5A68WGF6WM, G63QQF2NOX, V06SV4M95S, 4X49Y0596W
UPC 0637293029175
Application # M020
SPL Set ID 1c37b8d7-de72-f534-e063-6294a90aeab7
DEA schedule Non-controlled
Marketing category OTC MONOGRAPH DRUG
Marketing status On market
FDA listing status Listed (active directory)
Marketing start 2024-02-12
Route TOPICAL
Dosage form SPRAY
Substance OCTOCRYLENE; AVOBENZONE; HOMOSALATE; OCTISALATE
Why two NDCs? The FDA registers this code as 62670-6689-0 — a 5-4-1 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 package segment → 62670-6689-00. 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 spray sunscreen marketed as an over-the-counter monograph product. It contains four ultraviolet (UV) filter ingredients: avobenzone, homosalate, octisalate, and octocrylene. These chemicals are typically used together in sunscreen formulations to absorb and scatter UV radiation from the sun. The product is intended to be sprayed onto the skin as a sun-protective agent.

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.
Try another pack size: 53 mg
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
62670-6689-00 You're viewing this Main listing 117 mg in 1 CAN 2024-02-12 — Active
62670-6689-01 62670-6689-1 53 mg in 1 CAN 2025-02-10 — Active

You're viewing the largest of 2 pack sizes for this product.

Pack size FAQ

What quantity is in this package?
This package contains 117 mg — 117 mg in 1 can.
How does this package differ from NDC 62670-6689-01?
Both are Bath and Body Works SPF Waikiki Beach Coconut Avobenzone,Homosalate,Octisalate,Octocrylene 10 mg/100mg; 3 mg/100mg; 10 mg/100mg; 5 mg/100mg Spray — the drug itself is identical. This page's package is the 117 mg one, while NDC 62670-6689-01 is the 53 mg package.
What NDC number is used to bill for this package of Bath and Body Works SPF Waikiki Beach Coconut Avobenzone,Homosalate,Octisalate,Octocrylene 10 mg/100mg; 3 mg/100mg; 10 mg/100mg; 5 mg/100mg Spray?
Use the 11-digit billing form listed in the identifiers section of this page. Pharmacy and medical claims use the 11-digit form; the FDA label may print a shorter form of the same code.

Therapeutic equivalents

ProductLabelerPackNADAC/unitTEStatusPrice vs. this
Bath and Body Works SPF At The Beach 10 mg/100mg; 3 mg/100mg; 10 mg/100mg; 5 mg/100mg 62670-6690-00 Bath 53 mg — — FDA listed —
Bath and Body Works SPF Tahiti Isle 10 mg/100mg; 3 mg/100mg; 10 mg/100mg; 5 mg/100mg 62670-6858-00 Bath 117 mg — — FDA listed —
Bath and Body Works SPF Pink Pineapple Sunrise 10 mg/100mg; 3 mg/100mg; 10 mg/100mg; 5 mg/100mg 62670-6687-00 Bath 117 mg — — FDA listed —
Bath and Body Works SPF Waikiki Beach Coconut 10 mg/100mg; 3 mg/100mg; 10 mg/100mg; 5 mg/100mgthis 62670-6689-00 Bath 117 mg — — 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

🏛️
2024
On the market since
Feb 2024
📍
2026
Currently FDA-listed
2 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 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.

1 inactive ingredient listed in the exact product block matched to this NDC.

The official label also statesAlcohol Denat., Acrylates/Octylacrylamide Copolymer, Diethylhexyl 2,6-Naphthalate, Butyloctyl Salicylate, Dimethicone, Fragrance (Parfum), Tocopheryl Acetate, Hydroxycitronellal, Vanillin, Benzyl Salicylate, Coumarin, Geranyl Acetate, Pinene, Limonene, Citrus Aurantium Bergamia Peel Oil, Alpha-Isomethyl Ionone, Citrus Limon Peel Oil, Hexamethylindanopyran, Linalyl Acetate, Citronellol, Linalool.

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

LabelerBath & Body Works, Inc.
FDA applicationM020 (OTC MONOGRAPH DRUG)
Labeler code62670
First marketedFeb 2024
Product typeHuman Otc Drug
Portfolio402 products on file

More NDCs from Bath & Body Works, Inc. labeler code 62670

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 📄 When Using This Product 📄 Stop Use and Ask a Doctor If 📄 Keep Out of Reach of Children 📄 Package Label / Principal Display Panel
🎯 Indications and Usage 32 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 146 words ▾

Directions •Shake well before use. •Spray liberally and spread evenly by hand 15 minutes before sun exposure •Hold container 4-6 inches from skin to apply •Do not spray directly into face. Spray on hands then apply to face. •Do not apply in windy conditions •Use in a well ventilated area and avoid inhalation • 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 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 • children under 6 months: Ask a doctor

⚠️ Warnings 84 words ▾

Warnings For external use only Flammable. Do not use in the presence of a flame or spark. Keep away from sources of ignition -- No smoking. Do not use on damaged or broken skin When using this product keep out of eyes. Rinse with water to remove. keep away from face to avoid breathing in Stop use and ask a doctor if rash occurs Keep out of reach of children If product is swallowed, get medical help or contact a Poison Control Center immediately.

🧪 Active Ingredient 10 words ▾

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

🧪 Inactive Ingredients 40 words ▾

Inactive ingredients Alcohol Denat., Acrylates/Octylacrylamide Copolymer, Diethylhexyl 2,6-Naphthalate, Butyloctyl Salicylate, Dimethicone, Fragrance (Parfum), Tocopheryl Acetate, Hydroxycitronellal, Vanillin, Benzyl Salicylate, Coumarin, Geranyl Acetate, Pinene, Limonene, Citrus Aurantium Bergamia Peel Oil, Alpha-Isomethyl Ionone, Citrus Limon Peel Oil, Hexamethylindanopyran, Linalyl Acetate, Citronellol, Linalool.

🎯 Purpose 2 words ▾

Purpose Sunscreen

📄 Do Not Use 29 words ▾

Flammable. Do not use in the presence of a flame or spark. Keep away from sources of ignition -- No smoking. Do not use on damaged or broken skin

📄 When Using This Product 21 words ▾

When using this product keep out of eyes. Rinse with water to remove. keep away from face to avoid breathing in

📄 Stop Use and Ask a Doctor If 9 words ▾

Stop use and ask a doctor if rash occurs

📄 Keep Out of Reach of Children 20 words ▾

Keep out of reach of children If product is swallowed, get medical help or contact a Poison Control Center immediately.

📄 Package Label / Principal Display Panel 17 words ▾

Principal Display Panel Sunscreen Spray WBC spf 50 spray WBC FS SPF 50 spray WBC mini spf

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 Bath & Body Works, 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 1 other package presentation of this same product, including 53 mg (62670-6689-01). 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?
Bath & Body Works, 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.
← 62670-6688-00 · Bath 62670-6690-00 · Bath →
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.