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WISH HAND SANITIZER pink dragon biossom Alcohol 70 mL/100mL Spray, 50 mL — NDC 85537-0210-01 package photo
Label image from the product's FDA listing (DailyMed) — may show a different pack size or an older label revision.

WISH HAND SANITIZER pink dragon biossom Alcohol 70 mL/100mL Spray, 50 mL — NDC 85537-210-01 (Billing 85537-0210-01)

by PT SUPER HOME PRODUCT INDONESIA · 50 mL in 1 BOTTLE, SPRAY

This is a package of 50 mL of WISH HAND SANITIZER pink dragon biossom Alcohol 70 mL/100mL Spray from PT SUPER HOME PRODUCT INDONESIA, no longer marketed (first marketed Aug 2026), no longer in the FDA NDC Directory. It is this product's only package size.

NDC 85537-0210-01
🏷️ FDA NDC (as labeled) 85537-210-01 billing pads the product segment with a zero
OTC Discontinued Non-controlled ⚠ Discontinued by firm ⇄ Compare with another NDC
🗂️ FDA directory synced Oct 8, 2026 · this listing last changed Aug 20, 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 85537-210-01 alone.

Record
FDA NDC Directory package listing · Human OTC drug
Code segments
85537 labeler · 210 product · 01 package
Package marketed since
Aug 17, 2026
Sample package
No — commercial package
Listing certified through
Dec 31, 2027
Barcode (UPC-A, from the NDC)
3 8553721001 7
FDA record last changed
Aug 20, 2026
⚠️
Excluded from the active FDA NDC Directory. The labeler reported this product as discontinued, so it is excluded from the active NDC Directory. The listing was last certified through Aug 2026. 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) 85537-210-01
Product NDC 85537-210
11-digit billing NDC 85537021001
UNII 3K9958V90M
Application # M005
SPL Set ID 593b3fbe-a8de-1c09-e063-6294a90adc69
DEA schedule Non-controlled
Marketing category OTC MONOGRAPH DRUG
Marketing status Discontinued
FDA listing status Discontinued by firm (certified through Aug 2026)
Marketing start 2026-08-17
Route TOPICAL
Dosage form SPRAY
Substance ALCOHOL
Why two NDCs? The FDA registers this code as 85537-210-01 — 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 → 85537-0210-01. 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

📗 Our plain-language guide HelloPharmacist
  • It depends on the product. Hand sanitizers and wipes help reduce bacteria on your skin, and alcohol pads prepare skin before an injection. A separate injected form is used by heart...
  • Most directions say to cover all surfaces of your hands and rub until dry. Sprays and wipes follow similar steps. Check your product's label, since directions differ a bit between...
  • Children under 6 should use hand sanitizer only with adult supervision to avoid swallowing. Keep all products out of reach of children. If someone swallows it, get medical help or...
  • Stop using it and ask a doctor if you get irritation and redness, or if your condition lasts more than 72 hours. Avoid broken skin and keep it out of your eyes. If it gets in your...
📖 Read our full Alcohol 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.
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
85537-0210-01 You're viewing this Main listing 50 mL in 1 BOTTLE, SPRAY 2026-08-17 — Discontinued by firm

Therapeutic equivalents

ProductLabelerPackNADAC/unitTEStatusPrice vs. this
Hand Sanitizer Madrid Muse 70 mL/100mL 75328-0111-11 CROWN 30 ml — — FDA listed —
ROAME Moisturizing Hand Sanitizer Cloud 999 70 mL/100mL 85154-0100-01 Roame 35 ml — — FDA listed —
Wish Hand Sanitizer Black Plum Vanilla 70 mL/100mL 85537-0103-01 PT. 35 ml — — FDA listed —
Hand Sanitizer Valencia Vibes 70 mL/100mL 75328-0112-12 CROWN 30 ml — — FDA listed —
Mhb Skin Hydrating Hand Sanitizer, Lily Mist 70 mL/100mL 85537-0116-04 PT 35 ml — — FDA listed —
MHB SKIN HYDRATING HAND SANITIZER, MELON MUSE 35ml 70 mL/100mL 75328-0200-02 CROWN 1 bottle — — FDA listed —
MHB SKIN HYDRATING HAND SANITIZER SANTAL WAVE 35ml 70 mL/100mL 75328-0211-02 CROWN 1 bottle — — FDA listed —
Wish Hand Sanitizer Violet Orchid Sandalwood 70 mL/100mL 85537-0104-02 PT. 35 ml — — FDA listed —
Wish Hand Sanitizer Sweet Guava Fresh Coconut 70 mL/100mL 85537-0106-04 PT 35 ml — — FDA listed —
Mhb Skin Hydrating Hand Sanitizer, Citrus Peel 70 mL/100mL 85537-0117-05 PT 35 ml — — FDA listed —
Wish Hand Sanitizer Golden Citrus 70 mL/100mL 85537-0109-07 PT 35 ml — — FDA listed —
MHB SKIN HYDRATING HAND SANITIZER SANTAL WAVE 35ml 70 mL/100mL 85537-0111-02 PT 35 ml — — FDA listed —
Hand Sanitizer Mar Bella 70 mL/100mL 75328-0114-14 CROWN 30 ml — — FDA listed —
Mhb Skin Hydrating Hand Sanitizer, Lily Mist 70 mL/100mL 75328-0213-02 CROWN 1 bottle — — FDA listed —
HAND SANITIZER Cucumber Melon 70 mL/100mL 85537-0150-15 PT 35 ml — — FDA listed —
Wish Hand Sanitizer Dragonfruit Jasmine 70 mL/100mL 85537-0107-05 PT 35 ml — — FDA listed —
Mhb Skin Hydrating Hand Sanitizer, Melon Muse 70 mL/100mL 85537-0115-03 PT 35 ml — — FDA listed —
Wish Hand Sanitizer Salted Caramel Pistachio 70 mL/100mL 85537-0110-08 PT 35 ml — — FDA listed —
HAND SANITIZER lsland Coconut 70 mL/100mL 85537-0130-13 PT 35 ml — — FDA listed —
HAND SANITIZER Watermelon Sugar 70 mL/100mL 85537-0160-16 PT 35 ml — — FDA listed —
Wish Hand Sanitizer Cucumber Melon 70 mL/100mL 85537-0105-03 PT 35 ml — — FDA listed —
Wish Hand Sanitizer Coconut Cream White Florals 70 mL/100mL 85537-0108-06 PT 35 ml — — FDA listed —
HAND SANITIZER Cherry Blossom 70 mL/100mL 85537-0140-14 PT 35 ml — — FDA listed —
Hand Sanitizer Mallorca Breeze 70 mL/100mL 75328-0113-13 CROWN 30 ml — — FDA listed —
WISH HAND SANITIZER Rose Woods 70 mL/100mL 85537-0202-01 PT 35 ml — — FDA listed —
WISH HAND SANITIZER Banana Cream Sugar 70 mL/100mL 85537-0203-01 PT 35 ml — — FDA listed —
WISH HAND SANITIZER Caramel Vanilla Popcorn 70 mL/100mL 85537-0204-01 PT 35 ml — — FDA listed —
WISH HAND SANITIZER pink dragon biossom 70 mL/100mLthis 85537-0210-01 PT 50 ml — — Discontinued —
WISH HAND SANITIZER Strawberry Musk 70 mL/100mL 85537-0205-01 PT 35 ml — — FDA listed —
WISH HAND SANITIZER Sea Salt Green Herbs 70 mL/100mL 85537-0206-01 PT 35 ml — — FDA listed —
WISH HAND SANITIZER cherry rouge 70 mL/100mL 85537-0209-01 PT 50 ml — — FDA listed —
WISH HAND SANITIZER Mango Coconut Cream 70 mL/100mL 85537-0201-01 PT 35 ml — — FDA listed —
WISH HAND SANITIZER Marshmallow Vanilla 70 mL/100mL 85537-0207-01 PT 35 ml — — FDA listed —
WISH HAND SANITIZER Lychee Vanilla Milk 70 mL/100mL 85537-0208-01 PT 35 ml — — FDA listed —
WISH HAND SANITIZER pink dragon blossom 70 mL/100mL 85537-0217-01 PT 50 ml — — FDA listed —
WISH HAND SANITIZER rose petal 70 mL/100mL 85537-0212-01 PT 50 ml — — FDA listed —
Wish Advanced Hand Sanitizer Sweetr Guava Fresh Coconut 70 mL/100mL 85537-0213-01 PT 236 ml — — FDA listed —
Wish Advanced Hand Sanitizer Black Plum Vanilla 70 mL/100mL 85537-0214-01 PT 236 ml — — FDA listed —
WISH HAND SANITIZER vanilla cream 70 mL/100mL 85537-0211-01 PT 50 ml — — FDA listed —
Wish Advanced Hand Sanitizer Dragonfruit Jasmine 70 mL/100mL 85537-0216-01 PT 236 ml — — FDA listed —
Wish Advanced Hand Sanitizer Salted Caramel Pistachio 70 mL/100mL 85537-0215-01 PT 236 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
Aug 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.

🧪 Avoiding an ingredient? See Alcohol 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.

From the label’s inactive-ingredient sectionWater(Aqua), Glycerin,Aminomethyl Propanol,Fragrance,Aloe Barbadensis Leaf Juice,Tocophery Acetate(Vitamin E).Red4，Red33

This is label-wide narrative text, not a normalized exact-product ingredient list. A label can cover multiple strengths or packages.

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

LabelerPT SUPER HOME PRODUCT INDONESIA
FDA applicationM005 (OTC MONOGRAPH DRUG)
Labeler code85537
First marketedAug 2026
Product typeHuman Otc Drug
Portfolio31 products on file

More NDCs from PT SUPER HOME PRODUCT INDONESIA labeler code 85537

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 📄 Keep Out of Reach of Children 📄 Package Label / Principal Display Panel
🎯 Indications and Usage 25 words ▾

When using this product: avoid contact with face, eyes, and broken skin.In case of eye contact, flush with plenty of water and seek medical advice.

⏱️ Dosage and Administration 25 words ▾

Directions: Spray onto hands and rub together until dry. Recommended for repeat use.children under 6 years of age should be superised when using this product.

⚠️ Warnings 12 words ▾

Warnings: For external use only. Flammable, keep away from fire or flame.

🧪 Active Ingredient 8 words ▾

Active Ingredients: Ethyl Alcohol 70% v/v Purpose: Antimicrobial

🧪 Inactive Ingredients 10 words ▾

Inactive Ingredients: Water(Aqua), Glycerin,Aminomethyl Propanol,Fragrance,Aloe Barbadensis Leaf Juice,Tocophery Acetate(Vitamin E).Red4，Red33

🎯 Purpose 14 words ▾

USE: Hand sanitizer to help reduce bacteria on the skin that may cause disease.

📄 Do Not Use 11 words ▾

Stop use and ask a doctor if: Irritation or redness develops.

📄 Keep Out of Reach of Children 17 words ▾

Keep out of reach of children: lf swallowed, get medical help or contact a Poison Control Center.

📄 Package Label / Principal Display Panel 1 words ▾

10

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 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) ✓ 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.
Who lists this product with the FDA?
PT SUPER HOME PRODUCT INDONESIA 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.
← 85537-0209-01 · PT 85537-0211-01 · PT →
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.