NDC codes

FDA NDC Directory
Product NDC (as listed)85379-113Labeler and product segments. Claims need a package NDC.
Product NDC at billing width85379-0113Add 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
85379-113-118537901131125 VIAL in 1 CARTON (85379-113-11) / 5 mL in 1 VIALMarketed from Apr 1, 2025
85379-113-128537901131260 VIAL in 1 CARTON (85379-113-12) / 4 mL in 1 VIALMarketed from Mar 15, 2026

How the 11-digit form is made: The product segment has 3 digits, so one leading zero is added to it (5-3-2 → 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

Brand name (proprietary)
Resp Ease
Generic name (nonproprietary)
sodium chloride
Active ingredients
Sodium chloride — 60 mg/mL
Dosage form
Liquid
Route
Nasal
Labeler
Venture Healthcare LtdNDC labeler code 85379
Product type
Over-the-counter drug
Marketing category
Unapproved drug (other)
Marketing start
Listing expires
Identifiers
Product ID 85379-113_4d278204-9333-aeb8-e063-6394a90a87a4SPL ID 4d278204-9333-aeb8-e063-6394a90a87a4SPL set ID 31b88e7c-eca0-5540-e063-6294a90a1b18UNII 451W47IQ8XUPC 5060461080039

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. Nasal products like this are usually dispensed by a pharmacy and billed by NDC.

NDC on a medical claim

N485379011311 followed by a unit qualifier and the quantity

Package 85379-0113-11. 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)

Uses : For dry nasal membranes

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 85379-113

What is NDC 85379-113?
85379-113 is the product NDC for Resp Ease (sodium chloride), Sodium chloride 60 mg/mL liquid, listed with the FDA by Venture Healthcare Ltd. It has 2 package NDCs, shown above in 10- and 11-digit form.
What drug is associated with this NDC?
Resp Ease (Sodium chloride).
What is the active ingredient?
Sodium chloride.
Who is the labeler?
Venture Healthcare Ltd, NDC labeler code 85379. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Resp Ease?
5 other product NDCs are listed under this name. See all Resp Ease NDCs.
Is there a related HCPCS / J-code?
Not in Med-Code's curated HCPCS directory. See Billing references above.

Other finished products listed under the same name: strengths, forms and labelers.

Other Resp Ease NDCs
ProductStrengthForm · routeLabelerProduct NDCPackage NDCs (11-digit)
Resp Easesodium chlorideSodium chloride 30 mg/mLLiquidNasalLaboratoire Unither43014-111243014-1112-0143014-1112-02
Resp Easesodium chlorideSodium chloride 60 mg/mLLiquidNasalLaboratoire Unither43014-111343014-1113-0143014-1113-02
Resp Easesodium chlorideSodium chloride 70 mg/mLLiquidNasalLaboratoire Unither43014-111443014-1114-0143014-1114-02
Resp Easesodium chlorideSodium chloride 30 mg/mLLiquidNasalVenture Healthcare Ltd85379-11285379-0112-1185379-0112-12
Resp Easesodium chlorideSodium chloride 70 mg/mLLiquidNasalVenture Healthcare Ltd85379-11485379-0114-1185379-0114-12

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