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Reduce Lip Lines Lip Repair Mask 13 g/100g; .4 g/100g Ointment, 20 g — NDC 84356-0007-01 package photo
Label image from the product's FDA listing (DailyMed) — may show a different pack size or an older label revision.

Reduce Lip Lines Lip Repair Mask 13 g/100g; .4 g/100g Ointment, 20 g — NDC 84356-007-01 (Billing 84356-0007-01)

by Guangzhou Yapeng Refinement Chemical Co., Ltd. · 20 g in 1 BOX, UNIT-DOSE

This is a package of 20 g of Reduce Lip Lines Lip Repair Mask 13 g/100g; .4 g/100g Ointment from Guangzhou Yapeng Refinement Chemical Co., Ltd., marketed since Jun 2025 and currently FDA-listed. It is this product's only package size.

NDC 84356-0007-01
🏷️ FDA NDC (as labeled) 84356-007-01 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 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 84356-007-01 alone.

Record
FDA NDC Directory package listing · Human OTC drug
Code segments
84356 labeler · 007 product · 01 package
Package marketed since
Jun 21, 2025
Sample package
No — commercial package
Listing certified through
Dec 31, 2026
Barcode (UPC-A, from the NDC)
3 8435600701 3
FDA record last changed
Jul 24, 2026

Identity & classification

Regulatory identifiers FDA, NLM and CMS codes for this package

FDA NDC (as labeled) 84356-007-01
Product NDC 84356-007
11-digit billing NDC 84356000701
UNII RUE8E6T4NB, L7T10EIP3A
Application # 505G(a)(3)
SPL Set ID 37fce9e6-adae-af3c-e063-6394a90a140b
DEA schedule Non-controlled
Marketing category OTC MONOGRAPH DRUG
Marketing status On market
FDA listing status Listed (active directory)
Marketing start 2025-06-21
Route TOPICAL
Dosage form OINTMENT
Substance ALOE VERA LEAF JUICE; MENTHOL
Why two NDCs? The FDA registers this code as 84356-007-01 — 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 → 84356-0007-01. 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 an over-the-counter topical ointment marketed under FDA's OTC monograph rules for lip care. It contains aloe vera leaf juice, typically used as a skin conditioning ingredient, and menthol, which is commonly used for its cooling and soothing sensations on the skin. The product is applied directly to the lips as a mask or repair 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 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
84356-0007-01 You're viewing this Main listing 20 g in 1 BOX, UNIT-DOSE 2025-06-21 — Active

Therapeutic equivalents

ProductLabelerPackNADAC/unitTEStatusPrice vs. this
Reduce Lip Lines 13 g/100g; .4 g/100gthis 84356-0007-01 Guangzhou 20 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
Jun 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.

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 WL0328HX19
    A natural plant-based wax derived from candelilla shrub leaves. It acts as a coating agent, hardener, and texture modifier to control how quickly the medicine releases and to improve the tablet or capsule's appearance and stability.
  • UNII FGL3685T2X
    Chamomile is a plant extract used in medications as a flavoring agent and for its mild soothing properties in formulations. It helps improve taste and aroma of the medicine.
  • UNII E5GY4I6YCZ
    A fragrant liquid extracted from cinnamon bark, used as a flavoring agent to improve the taste of medicines and make them more pleasant to take.
  • UNII Q9L0O73W7L
    Coconut oil is a natural fat extracted from coconut fruit. It's used in medicines as a lubricant, emollient, or carrier to help dissolve or deliver active ingredients smoothly through the formulation.
  • UNII RDS2V6DVY5
    A plant extract from grape seeds that contains natural compounds. Used in supplements and medicines as an antioxidant ingredient and to support product stability.
  • UNII S270N0TRQY
    Hyaluronic acid is a naturally occurring substance found in skin and joints. In medicines, it acts as a moisturizer and thickening agent to improve texture and help the product spread smoothly.
  • UNII 724GKU717M
    Jojoba oil is a natural liquid wax extracted from jojoba plant seeds. It's used in medicines as an emollient and lubricant to soften and smooth the product, and sometimes as a carrier or penetration enhancer.
  • UNII MHT97MG5P8
    Rosa canina seed oil is a plant-based oil extracted from wild rose seeds. It's used in medicines as an emollient and carrier, helping to soften formulations and distribute active ingredients evenly throughout the product.
  • UNII R0ZB2556P8
    Tocopherol is a form of vitamin E derived from plant oils. It acts as an antioxidant in medicines to prevent oils and fats from breaking down and spoiling during storage.
  • UNII Q74T35078H
    Vanilla is a flavoring ingredient extracted from vanilla orchid beans. It's added to medicines to improve taste and make them more pleasant to take, especially for children or patients who need liquid formulations.

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

The official label also statesCandelilla Wax, Coconut Oil, Chamomile Extract, Cinnamon Oil, ROSA CANINA SEED OIL, Hyaluronic Acid, Jojoba Oil, Tocopherol, Vanilla Extract, Grapeseed Extract

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

LabelerGuangzhou Yapeng Refinement Chemical Co., Ltd.
FDA application505G(a)(3) (OTC MONOGRAPH DRUG)
Labeler code84356
First marketedJun 2025
Product typeHuman Otc Drug
Portfolio7 products on file

More NDCs from Guangzhou Yapeng Refinement Chemical Co., Ltd. labeler code 84356

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 📄 Stop Use and Ask a Doctor If 📄 Keep Out of Reach of Children 📄 Recent Major Changes 📄 Package Label / Principal Display Panel
🎯 Indications and Usage 11 words ▾

Reduce Lip Lines Relieve & Repair Increase Elasticity Lip Plumping Brightening

⏱️ Dosage and Administration 33 words ▾

Apply thin layer to clean lips using fingertip Gently massage for 30 seconds to enhance absorption Use up to 4 times daily, preferably at bedtime For overnight repair: Apply thick layer before sleep

⚠️ Warnings 17 words ▾

If allergic to mint, cinnamon, or botanical oils,On bleeding or infected lip areas,In children under 2 years

📦 Storage and Handling 14 words ▾

Keep tightly closed at 15-30°C (59-86°F). Avoid heat above 40°C (104°F) and direct sunlight.

🧪 Active Ingredient 12 words ▾

ACTIVE INGEREDIENT SECTION Menthol (from Peppermint Oil) 0.4% Aloe Vera Gel 13%

🧪 Inactive Ingredients 21 words ▾

Candelilla Wax, Coconut Oil, Chamomile Extract, Cinnamon Oil, ROSA CANINA SEED OIL, Hyaluronic Acid, Jojoba Oil, Tocopherol, Vanilla Extract, Grapeseed Extract

🎯 Purpose 24 words ▾

Temporarily relieves pain from chapped lips,Forms a protective barrier to heal dry/cracked lips,Enhances lip elasticity and reduces visible wrinkles,Brightens lip tone and evens pigmentation

📄 When Using This Product 28 words ▾

Avoid contact with eyes. If contact occurs, rinse thoroughly with water Discontinue if burning sensation persists over 10 minutes Not for ingestion. If swallowed, seek medical help immediately

📄 Stop Use and Ask a Doctor If 19 words ▾

If allergic to mint, cinnamon, or botanical oils On bleeding or infected lip areas In children under 2 years

📄 Keep Out of Reach of Children 6 words ▾

If ingested, contact Poison Control Center

📄 Recent Major Changes 11 words ▾

Reduce Lip Lines Relieve & Repair Increase Elasticity Lip Plumping Brightening

📄 Package Label / Principal Display Panel 3 words ▾

PXCKAGE LABEL label

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 Guangzhou Yapeng Refinement Chemical Co., Ltd.. Listing status can change — the directory data on this page refreshes weekly.
Who lists this product with the FDA?
Guangzhou Yapeng Refinement Chemical Co., 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.
← 84356-0006-01 · Guangzhou 84361-0002-02 · Instock →
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.