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ETERNAL SPIRIT BEAUTY PAIN RELIEF WITH HEMP Menthol, Camphor 10 g/100g; 3 g/100g Cream, 57 g — NDC 70947-0131-02 package photo
Label image from the product's FDA listing (DailyMed) — may show a different pack size or an older label revision.

ETERNAL SPIRIT BEAUTY PAIN RELIEF WITH HEMP Menthol, Camphor 10 g/100g; 3 g/100g Cream, 57 g — NDC 70947-131-02 (Billing 70947-0131-02)

by Worldwide Cosmetics, Inc · 57 g in 1 JAR

This is a package of 57 g of ETERNAL SPIRIT BEAUTY PAIN RELIEF WITH HEMP Menthol, Camphor 10 g/100g; 3 g/100g Cream from Worldwide Cosmetics, Inc, marketed since Dec 2025 and currently FDA-listed. It is this product's only package size.

NDC 70947-0131-02
🏷️ FDA NDC (as labeled) 70947-131-02 billing pads the product segment with a zero
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 70947-131-02 alone.

Record
FDA NDC Directory package listing · Human OTC drug
Code segments
70947 labeler · 131 product · 02 package
Package marketed since
Dec 20, 2025
Sample package
No — commercial package
Listing certified through
Dec 31, 2027
Barcode (UPC-A, from the NDC)
3 7094713102 1
FDA record last changed
Aug 27, 2026

Identity & classification

Regulatory identifiers FDA, NLM and CMS codes for this package

FDA NDC (as labeled) 70947-131-02
Product NDC 70947-131
11-digit billing NDC 70947013102
UNII L7T10EIP3A, N20HL7Q941
Application # M017
SPL Set ID 459d64a9-0538-57c8-e063-6394a90a6155
DEA schedule Non-controlled
Marketing category OTC MONOGRAPH DRUG
Marketing status On market
FDA listing status Listed (active directory)
Marketing start 2025-12-20
Route TOPICAL
Dosage form CREAM
Substance MENTHOL, UNSPECIFIED FORM; CAMPHOR (NATURAL)
Why two NDCs? The FDA registers this code as 70947-131-02 — 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 → 70947-0131-02. 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 cream containing menthol and camphor, marketed as an over-the-counter pain relief product under FDA's OTC monograph rules. Menthol and camphor are counterirritants typically used in topical products to produce a cooling or warming sensation on the skin, which may provide temporary relief from minor muscle and joint discomfort. The product is applied directly to the skin over the affected area.

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
70947-0131-02 You're viewing this Main listing 57 g in 1 JAR 2025-12-20 — Active

Therapeutic equivalents

ProductLabelerPackNADAC/unitTEStatusPrice vs. this
Menthol, Camphor 10 g/100g; 3 g/100g 49283-0576-02 Chemco 57 g — — FDA listed —
Eternal Spirit Beauty Pain Relief With Hemp 10 g/100g; 3 g/100gthis 70947-0131-02 Worldwide 57 g — — FDA listed —
Menthol, Camphor 10 g/100g; 3 g/100g 72937-0300-16 SUNSET 462 g — — Discontinued —
Menthol, Camphor 10 g/100g; 3 g/100g 72937-0022-16 SUNSET 473 g — — FDA listed —
Menthol, Camphor 10 g/100g; 3 g/100g 72937-0010-02 SUNSET 57 g — — Discontinued —
Menthol, Camphor 10 g/100g; 3 g/100g 72937-0013-08 SUNSET 237 g — — FDA listed —
Eternal Spirit Beauty Painless Pain Relieving 10 g/100g; 3 g/100g 70947-0010-04 Worldwide 118 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

🏛️
2025
On the market since
Dec 2025
📍
2026
Currently FDA-listed
1 year 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.

What it looks like

Color green
One label can cover several strengths, so colors may be combined — always confirm a loose pill against the dispensed prescription label or a pharmacist.
Where does this data come from?
Physical description (imprint, shape, color, scoring, coating) from this product’s FDA Structured Product Labeling (SPL), mirrored from DailyMed / openFDA.

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 A7E6112E4N
    A form of vitamin E used as an antioxidant in medicines. It prevents oils and fats in the product from breaking down, helping maintain stability and shelf life.
  • UNII 20R035KLCI
    A synthetic polymer used as a thickener and gelling agent. In medicines, it helps create the proper texture and consistency of gels, creams, or solutions, and may help control how quickly the active ingredient is released.
  • UNII 7528N5H79B
    A liquid solvent derived from grain fermentation. In medicines, it dissolves active ingredients, helps preserve the product, and improves how the body absorbs the drug.
  • UNII OC116GRO69
    Buteth-3 is a synthetic compound derived from butyl alcohol combined with ethylene oxide chains. It works as an emulsifier and surfactant, helping mix oil and water-based ingredients together in liquid or gel formulations.
  • UNII 69VJ1LPN1S
    Cannabis sativa seed oil is a plant-based oil derived from hemp seeds. It's used in medicines as a carrier or emollient to help deliver active ingredients and improve product texture and absorption.
  • UNII FJ1H6M2JG9
    A blend of plant-derived fatty acids that helps dissolve and deliver active ingredients. It acts as a solvent and absorption enhancer in soft gelatin capsules and liquid formulations.
  • UNII 2DMT128M1S
    A waxy solid derived from plant or animal sources. It acts as an emulsifier to blend oil and water components, and also thickens the medicine to give it the right texture and consistency.
  • UNII 936JST6JCN
    Cetyl alcohol is a waxy, fatty substance derived from plant or animal sources. It acts as an emulsifier and thickener in medicines, helping blend oil and water components and giving products a smooth, creamy texture.
  • UNII H5RIZ3MPW4
    A chemical preservative used to prevent bacterial and fungal growth in medicines. It helps extend shelf life and maintain product safety during storage and use.
  • UNII MCU2324216
    A silicone-based oil that reduces foaming and helps ingredients mix evenly. It's used as an antifoaming agent and lubricant in tablets, capsules, and liquid formulations.
  • UNII H3R47K3TBD
    FD&C Blue No. 1 is a synthetic blue dye approved for use in foods and medicines. It serves as a colorant to give the medication its distinctive appearance and help with product identification.
  • UNII I753WB2F1M
    FD&C Yellow No. 5 is a synthetic yellow colorant approved by the FDA. It is added to medicines to make pills, tablets, or liquids visually distinct and easier to identify.
  • UNII NNE56F2N14
    A synthetic compound derived from glycerin and polyethylene glycol. It acts as an emulsifier and solubilizer to help mix water and oil-based ingredients and keep them blended throughout the product's shelf life.
  • 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 FCZ5MH785I
    A waxy substance made from glycerin and stearic acid. It works as an emulsifier to help mix oil and water ingredients together, and as a thickener to give the medicine its proper texture and consistency.
  • UNII YSE9PPT4TH
    Hyaluronate sodium is a natural carbohydrate that holds moisture. It's used in medicines as a lubricant, thickener, and moisture-retaining agent to improve texture and delivery of the active ingredient.
  • UNII RMB44WO89X
    Hydroxyproline is an amino acid derived from collagen. In medications, it serves as a structural component or filler that may help provide stability and texture to the formulation.
  • UNII A2I8C7HI9T
    Methylparaben is a preservative derived from benzoic acid that prevents growth of bacteria, fungi, and mold in medicines. It extends the product's shelf life and maintains safety during storage.
  • UNII T5L8T28FGP
    Mineral oil is a clear, odorless liquid derived from crude oil. It acts as a lubricant and emollient in medications, helping pills slide smoothly during manufacturing and aiding moisture retention in topical products.
  • 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 7T1F30V5YH
    A synthetic emulsifier derived from sorbitol and oleic acid. It helps mix oil and water-based ingredients together and keeps them from separating in liquid formulations.
  • UNII Z8IX2SC1OH
    Propylparaben is a chemical preservative used to prevent bacterial and fungal growth in medicines and personal care products. It helps extend shelf life and maintain product safety during storage.
  • UNII 0LA2QC9O3Z
    A synthetic chemical compound used as a preservative and antioxidant in medicines. It helps prevent degradation of the active ingredients and extends the product's shelf life.
  • UNII JW3VT57I11
    A plant-based cleaning agent derived from coconut oil and wheat proteins. It acts as a surfactant and emulsifier to help mix ingredients and improve texture in the formulation.
  • UNII 4ELV7Z65AP
    Stearic acid is a fatty acid derived from plant or animal sources. It acts as a binder and lubricant in tablets and capsules, helping them hold together and flow smoothly during manufacturing.
  • UNII H8FJJ6KX5Y
    A plant extract from comfrey, used as a natural emollient and skin-conditioning agent in topical formulations to help soften and soothe the product texture.
  • UNII 827D5B1B6S
    Tributyl citrate is a clear, colorless liquid derived from citric acid. It works as a plasticizer in film coatings around tablets and capsules, making them flexible and less brittle so they dissolve properly.
  • UNII 3T5PCR2H0C
    A synthetic detergent and emulsifier made from plant-derived materials. It helps mix oil and water components together and improves how the medicine spreads or absorbs in the body.
  • 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.

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

The official label also statesWater (Aqua), Alcohol Denat, Stearic Acid, Paraffinum Liquidum, Cetearyl Alcohol, Polysorbate 60, Cetyl Alcohol, Dimethicone, Glyceryl Stearate, Acrylamide/Sodium Acrylate Copolymer, Trideceth-6, Glycereth-26, Tocopheryl Acetate, Caprylic/Capric Triglyceride, Propylene Glycol, Diazolidinyl Urea, Stearyl Alcohol, Polysorbate 20, Triethanolamine, Cannabis Sativa Seed Oil, Sodium Hyaluronate, Sodium PCA, Wheat Amino Acids, Panthenol, Symphytum Officinale (Comfrey) Extract, Hydroxyproline, Benzotriazolyl Dodecyl p-Cresol, Methylparaben, Propylparaben, FD&C YELLOW No.5 (CI 19140), FD&C Blue No.1 (CI 42090).

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

LabelerWorldwide Cosmetics, Inc
FDA applicationM017 (OTC MONOGRAPH DRUG)
Labeler code70947
First marketedDec 2025
Product typeHuman Otc Drug
Portfolio3 products on file

More NDCs from Worldwide Cosmetics, Inc labeler code 70947

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 📦 Storage and Handling 🧪 Active Ingredient 🧪 Inactive Ingredients 🎯 Purpose 📄 When Using This Product 📄 Keep Out of Reach of Children 📄 Questions or Comments 📄 Package Label / Principal Display Panel
🎯 Indications and Usage 22 words ▾

Uses For the temporary relief of minor aches and pains of muscles and joints associated with simple backache, arthritis, sprains and strains.

⏱️ Dosage and Administration 49 words ▾

Directions Adults and children over 12 years of age; apply a thin layer to affected area and rub gently not more than 3 to 4 times a day. Wash hands with soap and water after use. Children under 12 years of age; do not use unless directed by doctor/physician

⚠️ Warnings 57 words ▾

Use only as directed. For external use only. Do not bandage tightly. Do not use with heating pad, pack, wrap, hot water bottle or any heating element. Keep away from children. Package not child resistant. In case of accidental ingestion, contact doctor immediately. If prone to allergic reaction to the product, consult to a doctor before using.

📦 Storage and Handling 12 words ▾

Other information Store at room temperature 15° - 30°C (59° - 86°F)

🧪 Active Ingredient 4 words ▾

Menthol 10% Camphor 3%

🧪 Inactive Ingredients 69 words ▾

Inactive ingredients Water (Aqua), Alcohol Denat, Stearic Acid, Paraffinum Liquidum, Cetearyl Alcohol, Polysorbate 60, Cetyl Alcohol, Dimethicone, Glyceryl Stearate, Acrylamide/Sodium Acrylate Copolymer, Trideceth-6, Glycereth-26, Tocopheryl Acetate, Caprylic/Capric Triglyceride, Propylene Glycol, Diazolidinyl Urea, Stearyl Alcohol, Polysorbate 20, Triethanolamine, Cannabis Sativa Seed Oil, Sodium Hyaluronate, Sodium PCA, Wheat Amino Acids, Panthenol, Symphytum Officinale (Comfrey) Extract, Hydroxyproline, Benzotriazolyl Dodecyl p-Cresol, Methylparaben, Propylparaben, FD&C YELLOW No.5 (CI 19140), FD&C Blue No.1 (CI 42090).

🎯 Purpose 4 words ▾

External Analgesic Pain Relieving

📄 When Using This Product 31 words ▾

Avoid contact with eyes, mucous membranes, rashes, wounds or damaged skin. Do not apply on nose and genital area. If rash, redness or itchiness results; discontinue use and consult a doctor.

📄 Keep Out of Reach of Children 16 words ▾

Keep away from children. Package not child resistant. In case of accidental ingestion, contact doctor immediately.

📄 Questions or Comments 6 words ▾

Questions or comments? Contact us +1-305-4688790

📄 Package Label / Principal Display Panel 16 words ▾

ETERNAL SPIRIT BEAUTY PAIN RELIEF CREAM WITH HEMP OIL 3000 2 fl oz PAIN RELIEF CREAM

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 Worldwide Cosmetics, Inc. Listing status can change — the directory data on this page refreshes weekly.
Who lists this product with the FDA?
Worldwide Cosmetics, 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.
← 70947-0130-02 · Worldwide 70951-0123-01 · Laurel →
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.