Home › NDC Lookup › Ingredients › Menthol › 66902-0015-16
Fast Freeze MENTHOL 100 mg/mL Spray, 1 g — NDC 66902-0015-16 package photo
Label image from the product's FDA listing (DailyMed) — may show a different pack size or an older label revision.

Fast Freeze MENTHOL 100 mg/mL Spray, 1 g — NDC 66902-015-16 (Billing 66902-0015-16)

by Natural Essentials Inc. · 1 g in 1 BOTTLE, PUMP

This is a package of 1 g of Fast Freeze MENTHOL 100 mg/mL Spray from Natural Essentials Inc., no longer marketed (first marketed Jan 2013), no longer in the FDA NDC Directory.

NDC 66902-0015-16
🏷️ FDA NDC (as labeled) 66902-015-16 billing pads the product segment with a zero
This package
Contains1 g Pack sizes5 compare ↓
Product page 66902-0015-04 Also comes in: 1 g 66902-015-04 1 g 66902-015-27 1 g 66902-015-44 12 bottles 66902-015-12
OTC Discontinued Non-controlled ⚠ Discontinued by firm ⇄ Compare with another NDC
🗂️ FDA directory synced Oct 8, 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 66902-015-16 alone.

Record
FDA NDC Directory package listing · Human OTC drug
Code segments
66902 labeler · 015 product · 16 package
Listing certified through
Dec 31, 2026
Barcode (UPC)
0012345678905, 0038481009694
FDA record last changed
Jul 24, 2026
⚠️
Other active recalls for Menthol (different manufacturers) — 1 · tap to view
These affect other manufacturers’ products for the same ingredient — not necessarily the exact NDC on this page.
Class II · Mar 20, 2026 — This recall is being initiated following FDA's recommendation based on certain observations noted during an August 15, 2025, inspection of the manufacturing facility that may bear on product quality. (Xiamen Kang Zhongyuan Biotechnology Co., Ltd.) · FDA recall D-0458-2026
Each entry is an official FDA enforcement report — look up any recall number in the FDA recall database ↗
⚠️
Excluded from the active FDA NDC Directory. The labeler reported this product as discontinued, so it is excluded from the active NDC Directory. 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) 66902-015-16
Product NDC 66902-015
11-digit billing NDC 66902001516
RxCUI 667889, 1365995
UNII L7T10EIP3A
UPC 0012345678905, 0038481009694
Application # M017
SPL Set ID d8c42c8d-6ce0-43bf-b165-41979f3d8f79
DEA schedule Non-controlled
Marketing category OTC MONOGRAPH DRUG
Marketing status Discontinued
FDA listing status Discontinued by firm
Marketing start 2013-01-01
Route TOPICAL
Dosage form SPRAY
Substance MENTHOL
Quick answers
  • RxCUI (RxNorm): 667889
Why two NDCs? The FDA registers this code as 66902-015-16 — 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 → 66902-0015-16. 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

📗 Our plain-language guide HelloPharmacist
  • Mostly for temporary relief of minor aches and pains in muscles and joints, like those from arthritis, backache, strains, sprains and bruises. Some products are for other things, s...
  • It depends on the product. Many creams, gels and patches are limited to about 3 to 4 times a day, and patches also have a time limit, often 8 hours. Follow your product label and a...
  • A brief burning feeling can happen when you first apply it and usually fades in several days. But if you get severe burning pain, swelling or blistering, stop using it and call you...
  • No. Don't use menthol products with a heating pad, and avoid local heat or direct sunlight on the area. Rare cases of serious burns have been reported.
📖 Read our full Menthol guide →

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: 1 g 1 g 1 g 12 bottles
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
66902-0015-04 66902-015-04 Main listing 1 g in 1 BOTTLE, PUMP 2013-01-01 — Active
66902-0015-16 You're viewing this 1 g in 1 BOTTLE, PUMP 2013-01-01 — Discontinued by firm
66902-0015-27 66902-015-27 1 g in 1 BOTTLE, PUMP 2013-01-01 — Discontinued by firm
66902-0015-44 66902-015-44 1 g in 1 CAN 2013-01-01 — Active
66902-0015-12 66902-015-12 12 BOTTLE in 1 CASE / 118 mL in 1 BOTTLE 2025-08-12 — Active

Pack size FAQ

What quantity is in this package?
This package contains 1 g — 1 g in 1 bottle, pump.
How does this package differ from NDC 66902-0015-04?
Both are Fast Freeze MENTHOL 100 mg/mL Spray — the drug itself is identical. This page's package is the 1 g one, while NDC 66902-0015-04 is the 1 g package.
What NDC number is used to bill for this package of Fast Freeze MENTHOL 100 mg/mL 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
Xpect Stopain Clinical 100 mg/mL 42961-0257-01 Cintas 88 ml — — FDA listed —
ActivICE 100 mg/mL 53329-0996-04 Medline 118 ml — — FDA listed —
Biofreeze 100 mg/mL 59316-0104-10 Reckitt 59 ml — — FDA listed —
Stopain Clinical Continuous 100 mg/mL 63936-9504-04 Troy 118 ml — — FDA listed —
Ralli Rapid Pain Relief 100 mg/mL 63936-9509-01 Troy 88 ml — — FDA listed —
Fast Freeze 100 mg/mLthis 66902-0015-16 Natural 1 g — — Discontinued —
Still Standing 100 mg/mL 66902-0167-15 Natural 15 ml — — FDA listed —
Icy Freeze 100 mg/mL 66902-0168-40 Natural 120 ml — — FDA listed —
Game On Sport 100 mg/g 66902-0325-34 Natural 96 g — — 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

🏛️
2013
On the market since
Jan 2013
📍
2026
Currently FDA-listed
13 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.

🧪 Avoiding an ingredient? See Menthol inactive ingredients by manufacturer: every current product's list side by side, so you can ask your pharmacy for the version that does not list it.

Loading inactive ingredients from the official FDA label in the background. No external source is being called by this page request.
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

LabelerNatural Essentials Inc.
FDA applicationM017 (OTC MONOGRAPH DRUG)
Labeler code66902
First marketedJan 2013
Product typeHuman Otc Drug
Portfolio5 products on file

More NDCs from Natural Essentials Inc. labeler code 66902

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 📄 Stop Use and Ask a Doctor If 📄 Keep Out of Reach of Children 📄 Questions or Comments 📄 Package Label / Principal Display Panel
🎯 Indications and Usage 19 words ▾

Uses Temporary relief of minor aches and pains of muscles and joints associated with: Simple backache Arthritis Strains Sprains

⏱️ Dosage and Administration 31 words ▾

Directions Adults/Children 2 years and older: Spray on the affected area not more than 3 to 4 times daily Shake well before use Children under 2 years old: Consult a physician.

⚠️ Warnings 132 words ▾

Warnings For external use only Flammable Keep away from excessive heat or open flame Avoid spraying in eyes Contents under pressure. Do not puncture or incinerate container. Do not store at temperature above 120°F (48°C) Do not use With heating pad or device With ointments, creams, sprays or liniments On wounds, damaged skin or irritated skin Ask a doctor before use if you Have sensitive skin Are pregnant or breastfeeding When using this product Avoid contact with eyes or mucous membranes Do not bandage tightly Stop use and ask a doctor if Condition worsens Symptoms persist for more than 7 days or clear up then reoccur again within a few days Irritation develops Keep out of reach of children.

If swallowed, get medical help or contact a Poison Control Center right away.

🧪 Active Ingredient 4 words ▾

Active ingredients Menthol 10%

🧪 Inactive Ingredients 18 words ▾

Inactive ingredients Aloe Barbadensis (Aloe Vera) Leaf Extract, Ilex Paraguariensis Leaf Extract,SDA-39c Alcohol, Tocopherol (Vitamin E) Acetate, Water

🎯 Purpose 4 words ▾

Purpose Cooling Pain Relief

📄 Do Not Use 21 words ▾

Do not use With heating pad or device With ointments, creams, sprays or liniments On wounds, damaged skin or irritated skin

📄 Ask a Doctor Before Use If 14 words ▾

Ask a doctor before use if you Have sensitive skin Are pregnant or breastfeeding

📄 When Using This Product 15 words ▾

When using this product Avoid contact with eyes or mucous membranes Do not bandage tightly

📄 Stop Use and Ask a Doctor If 28 words ▾

Stop use and ask a doctor if Condition worsens Symptoms persist for more than 7 days or clear up then reoccur again within a few days Irritation develops

📄 Keep Out of Reach of Children 19 words ▾

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

📄 Questions or Comments 8 words ▾

Questions? Call 317-228-1144 or visit www.Bell-Horn.com or www.fastfreeze.com

📄 Package Label / Principal Display Panel 103 words ▾

Principal Display Panel – Bottle Label FAST FREEZE ® Naturally Cool Pain Relieving Continuous Spray Helps to relieve Sore muscles Strains & sprains Joint pain …………………………………. Invigorating cooling menthol Greaseless & stain-free Natural ingredients include Vitamin E, Aloe & llex …………………………………. 4 oz (118 mL) Principal Display Panel – Bottle Label

Principal Display Panel - Pump Bottle Label 4 oz (118 mL) Fast Freeze® Naturally Cool Pain Relieving Spray Helps to relieve Sore muscles Strains & sprains Joint Pain ------------------------------____________________________ Invigorating, cooling menthol Greaseless & stain-free Natural ingredients include Vitamin E, Aloe & Ilex _______________________________________________ 4 oz (118 mL) Bottle Label 4 oz

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 Menthol — the ingredient across all brands.

Top reported reactions

Pain3,545
Fatigue3,324
Nausea3,269
Headache3,025
Dyspnoea2,471
Diarrhoea2,208
Pneumonia2,151

Reporter sex

0 reports
Reports over time (by year) — tap or hover for the count & year
2019 2021 2023 2026 5,728 2,446
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) — Not published for this NDC The labeler did not submit a structured excipient list, or no SPL is 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.
Does this product come in other package sizes?
Yes — the FDA directory lists 4 other package presentations of this same product, including 1 g (66902-0015-04), 1 g (66902-0015-27), 1 g (66902-0015-44). 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?
Natural Essentials 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.
← 66902-0000-01 · Natural 66902-0016-01 · Natural →
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.