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Body Oil for Stretch Marks Helianthus Annuus (Sunflower) Seed 0il ,Tocopherol,Adansonia Digitata Seed 0il,Moringa Oleifera Seed 0il,Theobroma cacao (Cocoa) Seed Butter,Echium Plantagineum Seed Oil,Sesamum Indicum (Sesame) 30000 mg/60mL; 1200 mg/60mL; 1200 mg/60mL; 1200 mg/60mL; 1200 mg/60mL; 1200 mg/60mL; 1200 mg/60mL Oil, 60 mL — NDC 84509-101-01 (Billing 84509-0101-01)

by Dongguan Xiaogoubeige trading company Ltd. · 60 mL in 1 BOTTLE

This is a package of 60 mL of Body Oil for Stretch Marks Helianthus Annuus (Sunflower) Seed 0il ,Tocopherol,Adansonia Digitata Seed 0il,Moringa Oleifera Seed 0il,Theobroma cacao (Cocoa) Seed Butter,Echium Plantagineum Seed Oil,Sesamum Indicum (Sesame) 30000 mg/60mL; 1200 mg/60mL; 1200 mg/60mL; 1200 mg/60mL; 1200 mg/60mL; 1200 mg/60mL; 1200 mg/60mL Oil from Dongguan Xiaogoubeige trading company Ltd., marketed since Jan 2026 and currently FDA-listed. It is this product's only package size.

NDC 84509-0101-01
🏷️ FDA NDC (as labeled) 84509-101-01 billing pads the product segment with a zero
OTC On market Non-controlled ⇄ Compare with another NDC
🗂️ FDA directory synced Oct 8, 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 84509-101-01 alone.

Record
FDA NDC Directory package listing · Human OTC drug
Code segments
84509 labeler · 101 product · 01 package
Package marketed since
Jan 28, 2026
Sample package
No — commercial package
Listing certified through
Dec 31, 2027
Barcode (UPC-A, from the NDC)
3 8450910101 8
FDA record last changed
Aug 27, 2026

Identity & classification

Regulatory identifiers FDA, NLM and CMS codes for this package

FDA NDC (as labeled) 84509-101-01
Product NDC 84509-101
11-digit billing NDC 84509010101
UNII 3W1JG795YI, R0ZB2556P8, 77MKL7AR5I, QX10HYY4QV, PIB7XBU8XW, REM6A5QMC0 +1 more
Application # M016
SPL Set ID 496af9a1-7249-622f-e063-6394a90aa284
DEA schedule Non-controlled
Marketing category OTC MONOGRAPH DRUG
Marketing status On market
FDA listing status Listed (active directory)
Marketing start 2026-01-28
Route TOPICAL
Dosage form OIL
Substance SUNFLOWER OIL; TOCOPHEROL; ADANSONIA DIGITATA SEED OIL; SESAME OIL; ECHIUM PLANTAGINEUM SEED OIL; MORINGA OLEIFERA SEED OIL; COCOA BUTTER
Why two NDCs? The FDA registers this code as 84509-101-01 — 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 → 84509-0101-01. 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 body oil marketed as an OTC monograph product for stretch marks. It contains a blend of plant-derived oils and butters, including sunflower, sesame, moringa, baobab, and borage seed oils along with cocoa butter and tocopherol (vitamin E). These oils and butters are commonly used in topical skincare products for their emollient properties, which help soften and moisturize the skin. The product is applied directly to the skin as a topical treatment.

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 eachPer 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
84509-0101-01 You're viewing this Main listing 60 mL in 1 BOTTLE 2026-01-28 — Active

Therapeutic equivalents

ProductLabelerPackNADAC/unitTEStatusPrice vs. this
Body Oil for Stretch Marks 30000 mg/60mL; 1200 mg/60mL; 1200 mg/60mL; 1200 mg/60mL; 1200 mg/60mL; 1200 mg/60mL; 1200 mg/60mLthis 84509-0101-01 Dongguan 60 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

🏛️
2026
On the market since
Jan 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.

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 QN83US2B0N
    Ascorbyl palmitate is a fat-soluble form of vitamin C used as an antioxidant in medicines. It prevents oils and fats in the product from breaking down and becoming less stable over time.
  • UNII 5EM498GW35
    A mixture of aromatic compounds used to add pleasant smell to the medicine. Fragrance helps mask unpleasant tastes or odors, making the medication easier to take.
  • UNII 0RE8K4LNJS
    Isopropyl myristate is an oily liquid made from coconut or palm oil. It's used in medicines as an emollient and penetration enhancer to help the medicine absorb through skin or improve spreadability in topical products.
  • UNII 834K0WOS5G
    A natural fat extracted from sunflower seeds. It acts as an emulsifier and lubricant in medicines, helping mix ingredients that don't normally blend together and allowing the product to flow smoothly during manufacturing.
  • UNII ZU5L4DKH78
    Surfactin is a natural surfactant, a substance produced by certain bacteria that helps liquids mix together. In medicines, it reduces surface tension and acts as an emulsifier or solubilizer to help distribute ingredients evenly throughout the product.

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

The official label also statesIsopropyl Myristate,Cocoyl Hydrolyzed Collagen, Lecithin, Ascorbyl Palmitate, Fragrance (Parfum)

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

LabelerDongguan Xiaogoubeige trading company Ltd.
FDA applicationM016 (OTC MONOGRAPH DRUG)
Labeler code84509
First marketedJan 2026
Product typeHuman Otc Drug

More NDCs from Dongguan Xiaogoubeige trading company Ltd. labeler code 84509

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 📋 Description 📄 When Using This Product 📄 Keep Out of Reach of Children 📄 Package Label / Principal Display Panel
🎯 Indications and Usage 24 words ▾

INDICATIONS & USAGE Suitable for all types of skin damage due to stretching of the skin.Massage liberally into skin twice dally. Reapply as needed.

⏱️ Dosage and Administration 6 words ▾

DOSAGE Approximately 0.2-0.4 oz each time.

⚠️ Warnings 14 words ▾

WARNINGS For external use only. Keep out of reach of children.Avoid contact with eyes.

🧪 Active Ingredient 37 words ▾

Active Ingredients Helianthus Annuus (Sunflower) Seed 0il 50% Tocopherol 2% Adansonia Digitata Seed 0il 2% Moringa Oleifera Seed 0il 2% Theobroma cacao (Cocoa) Seed Butter 2% Echium Plantagineum Seed Oil 2% Sesamum Indicum (Sesame) Seed 0il 2%

🧪 Inactive Ingredients 11 words ▾

Inactive Ingredients Isopropyl Myristate,Cocoyl Hydrolyzed Collagen, Lecithin, Ascorbyl Palmitate, Fragrance (Parfum)

🎯 Purpose 3 words ▾

Purpose Moisturise, Wrinkle

📋 Description 42 words ▾

Made with Natural Vitamin E (Tocopherol)

Manufacturer Guangzhou Senmai Biotechnology Co.,Ltd

Address 1-4/F, Building A, Guanger Intelligence Industrial Park, No.2 Qianyi East Road, Shiling Town, Huadu District, Guangzhou, China

Capacity 60ml/2.03 Fl.oz

Shelf Life 3 Years

Place of Origin Made in China

📄 When Using This Product 57 words ▾

CAUTION Skin sensitivity heightens during pregnancy. We advise testing this and all skin care products on a small area, such as the inner forearm,48 hours before first use. Do not use if signs of irritation or rash appear. After using the product, if irritation or rash appears, discontinue use. lf irritation or rash persists, consult your doctor.

📄 Keep Out of Reach of Children 19 words ▾

KEEP OUT OF REACH OF CHILDREN lf swallowed, get medical help or contact a Poison Control Center right away.

📄 Package Label / Principal Display Panel 1 words ▾

latel

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 — Not published for this NDC No photo available yet for this listing.
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 Dongguan Xiaogoubeige trading company Ltd.. Listing status can change — the directory data on this page refreshes weekly.
Who lists this product with the FDA?
Dongguan Xiaogoubeige trading company Ltd. 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.
← 84509-0034-01 · Guangdong 84509-0102-01 · Guangzhou →
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.