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AOAO Retinol Anti-aging Box Set Collagen,Butyrospermum Parkii (Shea) Butter Extract,Hyaluronic Acid,Caffeine,Simmondsia Chinensis (Jojoba) Seed Oil,Retinol. 2250 mg/45mL; 1800 mg/45mL; 2250 mg/45mL; 405 mg/45mL; 450 mg/45mL; 450 mg/45mL Liquid, 45 mL — NDC 84509-0032-01 package photo
Label image from the product's FDA listing (DailyMed) — may show a different pack size or an older label revision.

AOAO Retinol Anti-aging Box Set Collagen,Butyrospermum Parkii (Shea) Butter Extract,Hyaluronic Acid,Caffeine,Simmondsia Chinensis (Jojoba) Seed Oil,Retinol. 2250 mg/45mL; 1800 mg/45mL; 2250 mg/45mL; 405 mg/45mL; 450 mg/45mL; 450 mg/45mL Liquid, 45 mL — NDC 84509-032-01 (Billing 84509-0032-01)

by Guangdong Junhui Biotechnology Co., LTD · 45 mL in 1 BOTTLE, UNIT-DOSE

This is a package of 45 mL of AOAO Retinol Anti-aging Box Set Collagen,Butyrospermum Parkii (Shea) Butter Extract,Hyaluronic Acid,Caffeine,Simmondsia Chinensis (Jojoba) Seed Oil,Retinol. 2250 mg/45mL; 1800 mg/45mL; 2250 mg/45mL; 405 mg/45mL; 450 mg/45mL; 450 mg/45mL Liquid from Guangdong Junhui Biotechnology Co., LTD, marketed since Oct 2024 and currently FDA-listed. It is this product's only package size.

NDC 84509-0032-01
🏷️ FDA NDC (as labeled) 84509-032-01 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 84509-032-01 alone.

Record
FDA NDC Directory package listing · Human OTC drug
Code segments
84509 labeler · 032 product · 01 package
Package marketed since
Oct 21, 2024
Sample package
No — commercial package
Listing certified through
Dec 31, 2026
Barcode (UPC-A, from the NDC)
3 8450903201 5
FDA record last changed
Aug 27, 2026

Identity & classification

Regulatory identifiers FDA, NLM and CMS codes for this package

FDA NDC (as labeled) 84509-032-01
Product NDC 84509-032
11-digit billing NDC 84509003201
UNII S270N0TRQY, K49155WL9Y, 8JC99XGU4W, G2SH0XKK91, 3G6A5W338E, 724GKU717M
Application # M016
SPL Set ID 24fdc31b-5291-a649-e063-6394a90a9c65
Established class (EPC) Central Nervous System Stimulant; Methylxanthine
Physiologic effect Central Nervous System Stimulation
Chemical class Xanthines
DEA schedule Non-controlled
Marketing category OTC MONOGRAPH DRUG
Marketing status On market
FDA listing status Listed (active directory)
Marketing start 2024-10-21
Route TOPICAL
Dosage form LIQUID
Substance HYALURONIC ACID; SHEA BUTTER; COLLAGEN, SOLUBLE, FISH SKIN; RETINOL; CAFFEINE; SIMMONDSIA CHINENSIS (JOJOBA) SEED OIL
Why two NDCs? The FDA registers this code as 84509-032-01 — 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 → 84509-0032-01. 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 liquid product marketed as a set under FDA's OTC monograph rules. It contains retinol, collagen, hyaluronic acid, shea butter, and jojoba seed oil, ingredients commonly included in skincare formulations for their moisturizing and conditioning properties. The product also contains caffeine, a central nervous system stimulant sometimes used in topical products. This listing appears in the OTC monograph category but has not undergone individual FDA approval as a new drug application.

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.
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
84509-0032-01 You're viewing this Main listing 45 mL in 1 BOTTLE, UNIT-DOSE 2024-10-21 — Active

Therapeutic equivalents

ProductLabelerPackNADAC/unitTEStatusPrice vs. this
AOAO Retinol Anti-aging Box Set 2250 mg/45mL; 1800 mg/45mL; 2250 mg/45mL; 405 mg/45mL; 450 mg/45mL; 450 mg/45mLthis 84509-0032-01 Guangdong 45 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

🏛️
2024
On the market since
Oct 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 ZY81Z83H0X
    Aloe vera leaf is a plant extract derived from the aloe plant. It is used in medicines as a natural moisturizer and skin-soothing agent in topical formulations.
  • UNII 4YS74Q4G4J
    A plant extract from Centella asiatica containing natural compounds called triterpenoids. It's used as an active ingredient in some formulations for its purported skin-supporting properties, though it functions as a botanical additive rather than a structural component of the medicine.
  • 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 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.

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

The official label also statesWater,Glycerin,Aloe Barbadensis Leaf Extract，Centella Asiatica 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

LabelerGuangdong Junhui Biotechnology Co., LTD
FDA applicationM016 (OTC MONOGRAPH DRUG)
Labeler code84509
First marketedOct 2024
Product typeHuman Otc Drug
Portfolio4 products on file

More NDCs from Guangdong Junhui Biotechnology Co., 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 39 words ▾

Uses 1. Take out a bottle of essence from the box 2. Unscrew the top cap and squeeze the essence into the palm of your hand 3. Apply evenly on the face and neck, gently massage until fully moisturized

⏱️ Dosage and Administration 5 words ▾

DOSAGE Approximately 0.15fl.oz each time

⚠️ Warnings 13 words ▾

Warnings For external use only. Keep out ofreach of children.Avoid contact with eyes

🧪 Active Ingredient 23 words ▾

Active Ingredients Collagen 5% Butyrospermum Parkii (Shea) Butter Extract 4% Hyaluronic Acid 5% Caffeine 1% Simmondsia Chinensis (Jojoba) Seed Oil 1% Retinol 0.9%

🧪 Inactive Ingredients 8 words ▾

Inactive Ingredients Water,Glycerin,Aloe Barbadensis Leaf Extract，Centella Asiatica Extract.

🎯 Purpose 6 words ▾

Purpose Anti-wrinkle Nourish Moisturizing Firming Anti-aging

📋 Description 43 words ▾

Product Name AOAO Retinol Anti-aging Box Set

Manufacturer Guangdong Junhui Biotechnology Co., LTD

ADDRESS No. 10, Guangrui Street, Guangzhou (Qingyuan) Industrial Transfer Park, Shijiao Town, Qingcheng District, Qingyuan City, Guangdong Province

Capacity 1.5ml*30

Shelf Life 3 Years

Place of Origin Made in China

📄 When Using This Product 17 words ▾

CAUTION After using the product if irritation or rash appears,discontinue use.If irritation or rash persists.consult your doctor.

📄 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

📄 Package Label / Principal Display Panel 1 words ▾

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 Guangdong Junhui Biotechnology Co., LTD. Listing status can change — the directory data on this page refreshes weekly.
Who lists this product with the FDA?
Guangdong Junhui Biotechnology 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.
← 84509-0016-01 · Guangdong 84509-0034-01 · Guangdong →
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.