What is NDC 71489-006?

71489-006 is the product NDC for Sani Luxe Foaming Hand Sanitizer Alcohol Free, Benzalkonium chloride 1 mg/mL liquid, listed with the FDA by Celeste Industries Corporation. It has 16 package NDCs, shown above in 10- and 11-digit form.

What drug is associated with this NDC?

Sani Luxe Foaming Hand Sanitizer Alcohol Free (Benzalkonium chloride).

Celeste Industries Corporation, NDC labeler code 71489. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.

What other NDCs exist for Sani Luxe Foaming Hand Sanitizer Alcohol Free?

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.

NDC 71489-006

NDC codes

FDA NDC Directory

Product NDC (as listed)71489-006Labeler and product segments. Claims need a package NDC.

Product NDC at billing width71489-0006Add 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 NDC	11-digit (billing)	Package
71489-006-01	7148900060171489000601	237 mL in 1 BOTTLE, PUMP (71489-006-01)Marketed from Jan 28, 2019
71489-006-02	7148900060271489000602	56 mL in 1 BOTTLE, PUMP (71489-006-02)Marketed from Mar 25, 2020
71489-006-03	7148900060371489000603	177 mL in 1 BOTTLE (71489-006-03)Marketed from May 20, 2020
71489-006-04	7148900060471489000604	284 mL in 1 BOTTLE, PUMP (71489-006-04)Marketed from May 20, 2020
71489-006-05	7148900060571489000605	355 mL in 1 BOTTLE, PUMP (71489-006-05)Marketed from May 20, 2020
71489-006-06	7148900060671489000606	3785 mL in 1 BOTTLE (71489-006-06)Marketed from May 20, 2020
71489-006-07	7148900060771489000607	59 mL in 1 BOTTLE (71489-006-07)Marketed from Jun 25, 2020
71489-006-08	7148900060871489000608	177 mL in 1 BOTTLE, PUMP (71489-006-08)Marketed from Jun 25, 2020
71489-006-09	7148900060971489000609	237 mL in 1 BOTTLE (71489-006-09)Marketed from Jun 25, 2020
71489-006-10	7148900061071489000610	284 mL in 1 BOTTLE (71489-006-10)Marketed from Jun 25, 2020
71489-006-11	7148900061171489000611	355 mL in 1 BOTTLE (71489-006-11)Marketed from Jun 25, 2020
71489-006-12	7148900061271489000612	3785 mL in 1 BOTTLE, PUMP (71489-006-12)Marketed from Jun 25, 2020
71489-006-13	7148900061371489000613	946 mL in 1 BOTTLE (71489-006-13)Marketed from Jun 30, 2020
71489-006-14	7148900061471489000614	946 mL in 1 BOTTLE, PUMP (71489-006-14)Marketed from Jun 30, 2020
71489-006-15	7148900061571489000615	530 mL in 1 BOTTLE (71489-006-15)Marketed from Oct 14, 2020
71489-006-16	7148900061671489000616	530 mL in 1 BOTTLE, PUMP (71489-006-16)Marketed from Oct 14, 2020

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): Sani Luxe Foaming Hand Sanitizer Alcohol Free
Generic name (nonproprietary): benzalkonium chloride
Active ingredients: Benzalkonium chloride — 1 mg/mL
Dosage form: Liquid
Route: Cutaneous
Labeler: Celeste Industries CorporationNDC labeler code 71489
Product type: Over-the-counter drug
Marketing category: OTC monograph drugApplication 505G(a)(3)
Marketing start: Jan 28, 2019
Listing expires: Dec 31, 2026
Identifiers: Product ID 71489-006_1cbe491e-af31-8dd8-e063-6394a90ae2f5SPL ID 1cbe491e-af31-8dd8-e063-6394a90ae2f5SPL set ID 7549428e-b10f-45b9-b414-0c6e8b41c398RxCUI 1038799UNII F5UM2KM3W7

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 drug-specific HCPCS code in Med-Code's directory for this product. The directory is curated and not complete — check the current CMS HCPCS file before billing.

NDC on a medical claim

N471489000601 followed by a unit qualifier and the quantity

Package 71489-0006-01. 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 Jul 8, 2024.

Indications (excerpt from the label)

Uses Recommended for repeated use For hand sanitizing to decrease bacteria on the skin

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 71489-006

What is NDC 71489-006?: 71489-006 is the product NDC for Sani Luxe Foaming Hand Sanitizer Alcohol Free, Benzalkonium chloride 1 mg/mL liquid, listed with the FDA by Celeste Industries Corporation. It has 16 package NDCs, shown above in 10- and 11-digit form.
What drug is associated with this NDC?: Sani Luxe Foaming Hand Sanitizer Alcohol Free (Benzalkonium chloride).
What is the active ingredient?: Benzalkonium chloride.
Who is the labeler?: Celeste Industries Corporation, NDC labeler code 71489. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Sani Luxe Foaming Hand Sanitizer Alcohol Free?: 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.

Other NDCs under 505G(a)(3)

Products listed under the same FDA application: other strengths and forms, and repackagers who relabel the same product.

FDA NDC Directory listings under 505G(a)(3)
Product	Strength	Form · route	Labeler	Product NDC
Pretty Pump Hand Sanitizeralcohol	Alcohol 600 mL/L	SprayTopical	Whisk Products, Inc.	65585-489
Protec Hand Sani Gel Antibacterialalcohol	Alcohol .7 mL/mL	GelTopical	Degasa, S.A. de C.V.	67326-006
Foaming Antibacterialbenzalkonium chloride	Benzalkonium chloride 1.3 g/1000mL	SolutionTopical	Sam's West, Inc.	68196-667
Smart Care TEA and TIMBER HAND SANITIZERethyl alcohol	Alcohol 70 mL/100mL	SprayTopical	Ashtel Studios, Inc.	70108-199
B-Pure Moisturizing Hand Sanitizer Warm Cashmere Scentedalcohol	Alcohol 70 mL/100mL	LiquidTopical	Fourstar Group USA, Inc.	80684-217
VQ Hydrating Hand Sanitizer Frosted Candy Applealcohol	Alcohol 67.5 mL/100mL	LiquidTopical	Tychea Co.	85980-024
BCBG GENERATION HAND SANITIZER DUO - WILD Cherry AND Mango Cherry SCENTethyl alcohol	—	Kit	Diamond Life Cosmetics Trading FZCO	87247-933
Anti Bacterial Hand Gel Ginghamalcohol	Alcohol 71 mL/100mL	GelTopical	Bath & Body Works, Inc.	62670-6641
Anti Bacterial Hand Gel Disney Villains Evil Queenalcohol	Alcohol 71 mL/100mL	GelTopical	Bath & Body Works, Inc.	62670-6919
Povidone-Iodine Prep Winged Sterile Largepovidone-iodine	Povidone-iodine 100 mg/g	SpongeTopical	Cardinal Health 200, Inc	63517-759
Smart-San Hand Sanitizer Foamalcohol	Alcohol 74 mL/100mL	LiquidTopical	Best Sanitizers, Inc.	59900-352
BZK Antiseptic Towelette Sterilebenzalkonium chloride	Benzalkonium chloride 1.3 mg/g	ClothTopical	Jianerkang Medical Co., Ltd	34645-0018
Lavender Hand Sanitizing Wipesethanol	Alcohol 65 mL/100mL	ClothTopical	Whole Foods Market, Inc.	42681-6810
Pacific Blue ultra Antimicrobial Foam Fragrance Freebenzalkonium chloride	Benzalkonium chloride .13 g/100mL	SolutionTopical	Georgia-Pacific Consumer Products	54622-316
Zylast Antiseptic Sethyl alcohol	Alcohol 760 mL/1000mL	LiquidTopical	Innovative BioDefense	57362-466
WhiskCare 375alcohol	Alcohol 600 mL/L	GelTopical	Whisk Products, Inc.	65585-375
GuruNanda Healthy Gumscetylpyridinium chloride	Cetylpyridinium chloride 1 mg/mL	MouthwashOral	GURUNANDA, LLC	70708-926
Smart Care SWEET AND STILL HAND SANITIZERethyl alcohol	Alcohol 70 mL/100mL	SprayTopical	Ashtel Studios, Inc.	70108-192
B-Pure Moisturizing Hand Sanitizer Midnight Freesia Scentedalcohol	Alcohol 70 mL/100mL	LiquidTopical	Fourstar Group USA, Inc.	80684-214
RootStim Minoxidil Hair Regrowth Treatmentminoxidil	Minoxidil 5 g/100mL	LiquidTopical	YITONGBADA (SHENZHEN) INTERNATIONAL TRADE CO., LTD	83364-025

Showing 20 of 40.

Sani Luxe Foaming Hand Sanitizer Alcohol Free (Benzalkonium chloride) NDC 71489-006