NDC codes

FDA NDC Directory
Product NDC (as listed)84755-0005Labeler and product segments. Claims need a package NDC.
Product NDC at billing width84755-0005Add the package segment from the table below.
Package NDCs as listed with the FDA, and the 11-digit 5-4-2 form used on claims. The highlighted digit is the added leading zero.
Package NDC11-digit (billing)PackageCopy
84755-0005-184755000501847550005012 U in 1 BOTTLE (84755-0005-1)Marketed from Sep 1, 2025

How the 11-digit form is made: The package segment has 1 digit, so one leading zero is added to it (5-4-1 → 5-4-2). Formatting the NDC does not by itself make it billable — the product, package and quantity must match what was dispensed or administered, and payer rules apply. Conversion rules

Product information

Generic name (nonproprietary)
krx aesthetics biophase molecular night peel
Active ingredients
Salicyloyl phytosphingosine — 10 mg/UGluconolactone — 100 mg/U
Dosage form
Cream
Route
Topical
Labeler
KRX RESOURCES SDN. BHD.NDC labeler code 84755
Product type
Over-the-counter drug
Marketing category
Unapproved drug (other)
Marketing start
Listing expires
Other FDA classes
Irrigation (Mechanism)
Identifiers
Product ID 84755-0005_4173475d-c016-8ad3-e063-6394a90ad772SPL ID 4173475d-c016-8ad3-e063-6394a90ad772SPL set ID 3dd69bcb-3743-eb01-e063-6394a90ab7e0UNII U891J4JCNH, WQ29KQ9POT
Pharmacologic class
Calculi Dissolution Agent

Billing references

What Med-Code can say about coding this product, and where each statement comes from. Nothing here is inferred from the name alone.

HCPCS codeNo match

No HCPCS code in Med-Code's directory. Topical products like this are usually dispensed by a pharmacy and billed by NDC.

NDC on a medical claim

N484755000501 followed by a unit qualifier and the quantity

Package 84755-0005-01. Unit qualifiers: F2 (international unit), GR (gram), ME (milligram), ML (milliliter), UN (unit (each)). The qualifier and quantity depend on what was given. About the N4 qualifier

Product label

Current FDA label (SPL), effective .

Indications (excerpt from the label)

Indications and Usage KrX Aesthetics Biophase Molecular Night Peel (PHA/LHA) is indicated for topical use as an exfoliating treatment. Helps gently resurface the skin to improve texture, clarity, and brightness. Aids in the removal of dead skin cells while promoting a smoother, more radiant complexion. Recommended for use at night as part of a skincare regimen. Not intended for use on broken or inflamed skin.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 84755-0005

What is NDC 84755-0005?
84755-0005 is the product NDC for Krx Aesthetics Biophase Molecular Night Peel, Salicyloyl phytosphingosine 10 mg/U; Gluconolactone 100 mg/U cream, listed with the FDA by KRX RESOURCES SDN. BHD.. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?
Krx Aesthetics Biophase Molecular Night Peel.
What is the active ingredient?
Salicyloyl phytosphingosine, Gluconolactone.
Who is the labeler?
KRX RESOURCES SDN. BHD., NDC labeler code 84755. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Krx Aesthetics Biophase Molecular Night Peel?
None: this is the only finished product listed under this name.
Is there a related HCPCS / J-code?
Not in Med-Code's curated HCPCS directory. See Billing references above.

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