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LA FRESH Antiperspirant Wipe Aluminum Chlorohydrate 15% .15 g/g Cloth, 3 g — NDC 64709-160-10 (Billing 64709-0160-10) · Product 64709-160

by Diamond Wipes International, Inc · 3 g in 1 PACKET (64709-160-10)

NDC 64709-160-10 (billing 64709-0160-10) is a package of 3 g of LA FRESH Antiperspirant Wipe Aluminum Chlorohydrate 15% .15 g/g Cloth from Diamond Wipes International, Inc, no longer marketed (first marketed Jan 2019), no longer in the FDA NDC Directory. It is the main listing for product NDC 64709-160, its only package size.

NDC 64709-0160-10
🏷️ FDA NDC (as labeled) 64709-160-10 billing pads the product segment with a zero
OTC Discontinued Non-controlled ⚠ Discontinued by firm ⇄ 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

⚠️
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 Oct 2020. 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) 64709-160-10
Product NDC 64709-160
11-digit billing NDC 64709016010
UNII HPN8MZW13M
Application # M019
SPL Set ID b6fe78fb-474d-3d8f-e053-2a95a90a1fd7
DEA schedule Non-controlled
Marketing category OTC MONOGRAPH DRUG
Marketing status Discontinued
FDA listing status Discontinued by firm (certified through Oct 2020)
Marketing start 2019-01-01
Route TOPICAL
Dosage form CLOTH
Substance ALUMINUM CHLOROHYDRATE
Quick answers for NDC 64709-160-10
  • 11-digit billing NDC: 64709016010
Why two NDCs? The FDA registers this code as 64709-160-10 — 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 → 64709-0160-10. 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?

LA FRESH Antiperspirant Wipe is a cloth-based topical product containing aluminum chlorohydrate, an active ingredient commonly used in antiperspirant formulations. Aluminum chlorohydrate is typically used to reduce underarm perspiration by temporarily blocking sweat glands. This product is an over-the-counter monograph drug, meaning it follows FDA's established safety and effectiveness rules for the antiperspirant category rather than being individually approved 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 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
64709-0160-10 64709-160-10 You're viewing this Main listing 3 g in 1 PACKET (64709-160-10) 2019-01-01 — Discontinued by firm

Therapeutic equivalents

ProductLabelerPackNADAC/unitTEStatusPrice vs. this
LA FRESH Antiperspirant Wipe .15 g/gthis 64709-0160-10 Diamond 3 g — — Discontinued —
LA FRESH Antiperspirant Wipe .15 g/g 64709-0161-10 Diamond 36.58 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

🏛️
2019
On the market since
Jan 2019
📍
2026
Currently FDA-listed
7 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.

Loading inactive ingredients from the official FDA label in the background. No external source is being called by this page request.
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

LabelerDiamond Wipes International, Inc
FDA applicationM019 (OTC MONOGRAPH DRUG)
Labeler code64709
First marketedJan 2019
Product typeHuman Otc Drug
Portfolio4 products on file
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 📄 Keep Out of Reach of Children 📄 Package Label / Principal Display Panel
🎯 Indications and Usage 4 words ▾

Use reduce underarm perspiration

⏱️ Dosage and Administration 11 words ▾

Directions ■open packet ■remove and unfold wipe ■apply to underarm only

⚠️ Warnings 28 words ▾

Warnings For external use only Do not use on broken skin Stop use if rash or irritation occurs Ask a doctor before use if you have kidney disease

🧪 Active Ingredient 5 words ▾

Active ingredient Aluminum Chlorohydrate 15%

🧪 Inactive Ingredients 29 words ▾

Inactive ingredients Benzoic Acid, Benzyl Alcohol, Chlorphenesin, Fragrance, PEG-180, Phenoxyethanol, Polysorbate 20, Potassium Sorbate, Salvia Officinalis (Sage) Leaf Extract, Sorbic Acid, Tocopherol, Tocopheryl Acetate, Usnea Barbata (Lichen) Extract, Water

🎯 Purpose 2 words ▾

Purpose Antiperspirant

📄 Keep Out of Reach of Children 25 words ▾

Keep out of reach of children Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away

📄 Package Label / Principal Display Panel 155 words ▾

Label OMG IT'S YOU NO SWEAT ANTIPERSPIRANT WIPE Do Not Flush LA Fresh ® NO SWEAT ANTIPERSPIRANT WIPE @LAFreshgroup // www.LAFreshgroup.com Drug Facts Active ingredient (in each wipe) Purpose Aluminum Chlorohydrate 15%...................................Antiperspirant Use reduce underam perspiration Warnings For external use only. Do not use on broken skin. Stop use if rash or irritation occurs.

Ask a doctor before use if you have kidney disease Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away Directions ■open packet ■remove and unfold wipe ■apply to underarm only Inactive ingredients Benzoic Acid, Benzyl Alcohol, Chlorphenesin, Fragrance, PEG-180, Phenoxyethanol, Polysorbate 20, Potassium Sorbate, Salvia Officinalis (Sage) Leaf Extract, Sorbic Acid, Tocopherol, Tocopheryl Acetate, Usnea Barbata (Lichen) Extract, Water // Contains 1 wipe MADE IN USA WITH DOMESTIC AND IMPORTED PARTS for LA Fresh Group, Inc., Chino, CA 91710 ®™© 2022 LA Fresh Group FSC MIX Paper FSC ® C109834 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 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 — Not published for this NDC No photo available yet for this listing.
Inactive ingredients (structured) — Not published for this NDC The labeler did not submit a structured excipient list, or no SPL is 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 FDA registers it as 64709-160-10, which is what is printed on the packaging and shown on DailyMed. Insurance claims use a fixed 11-digit 5-4-2 format, so the short segment is padded with a leading zero: 64709-0160-10, written without dashes as 64709016010. The Identity section at the top of this page lists every form of this code.
What do the three segments of this NDC mean?
In 64709-0160-10, the first segment (64709) is the labeler code FDA assigned to Diamond Wipes International, Inc; the middle segment (0160) identifies this specific product — its ingredient, strength, and dosage form; and the last segment (10) identifies this exact package size and type. Together they name one specific package of one specific product.
Who lists this product with the FDA?
Diamond Wipes International, 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.
← 64709-0120-01 · Diamond 64709-0161-10 · Diamond →
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.