What is NDC 37945-902?

37945-902 is the product NDC for Antimicrobial Face Body Wash (benzethonium chloride liquid), Benzethonium chloride .2 g/100g liquid, listed with the FDA by Bio-Medical & Pharmaceutical Manufacturing Corporation. It has 1 package NDC, shown above in 10- and 11-digit form.

What drug is associated with this NDC?

Antimicrobial Face Body Wash (Benzethonium chloride liquid).

Bio-Medical & Pharmaceutical Manufacturing Corporation, NDC labeler code 37945. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.

What other NDCs exist for Antimicrobial Face Body Wash?

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.

Antimicrobial Face Body Wash NDC 37945-902

NDC codes

FDA NDC Directory

Product NDC (as listed)37945-902Labeler and product segments. Claims need a package NDC.

Product NDC at billing width37945-0902Add 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	Copy
37945-902-08	3794509020837945090208	236 g in 1 BOTTLE (37945-902-08)Marketed from Oct 9, 2015

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): Antimicrobial Face Body Wash
Generic name (nonproprietary): benzethonium chloride liquid
Active ingredients: Benzethonium chloride — .2 g/100g
Dosage form: Liquid
Route: Topical
Labeler: Bio-Medical & Pharmaceutical Manufacturing CorporationNDC labeler code 37945
Product type: Over-the-counter drug
Marketing category: OTC monograph (not final)Application part333E
Marketing start: Oct 9, 2015
Listing expires: Dec 31, 2026
Identifiers: Product ID 37945-902_a346ebd2-fc2e-b574-e053-2995a90a0d3aSPL ID a346ebd2-fc2e-b574-e053-2995a90a0d3aSPL set ID 210dc091-4a9b-0c48-e054-00144ff88e88RxCUI 1243889UNII PH41D05744

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

N437945090208 followed by a unit qualifier and the quantity

Package 37945-0902-08. 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 Apr 15, 2020.

Indications (excerpt from the label)

Use A unique, non-drying cleanser. Developed for all skin types and pH balanced. Helps 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 37945-902

What is NDC 37945-902?: 37945-902 is the product NDC for Antimicrobial Face Body Wash (benzethonium chloride liquid), Benzethonium chloride .2 g/100g liquid, listed with the FDA by Bio-Medical & Pharmaceutical Manufacturing Corporation. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?: Antimicrobial Face Body Wash (Benzethonium chloride liquid).
What is the active ingredient?: Benzethonium chloride.
Who is the labeler?: Bio-Medical & Pharmaceutical Manufacturing Corporation, NDC labeler code 37945. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Antimicrobial Face Body Wash?: 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 part333E

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

FDA NDC Directory listings under part333E
Product	Strength	Form · route	Labeler	Product NDC
Afassco Hand Sanitizeralcohol	Alcohol 62 mL/100mL	LiquidTopical	JIANGMEN SHUIZIRUN SANITARY ARTICLES CO., LTD.	71734-206
Alcohol Wipesalcohol	Alcohol .31 mL/mL	ClothTopical	JIANGMEN SHUIZIRUN SANITARY ARTICLES CO., LTD.	71734-202
DEFENSE Hand Sanitizerisopropyl alcohol	Isopropyl alcohol .75 mL/mL	LiquidTopical	Walla Walla Environmental, Inc.	80579-000
DEFENSE Hand Sanitizerisopropyl alcohol	Isopropyl alcohol .75 mL/mL	LiquidTopical	Walla Walla Environmental, Inc.	80579-001
Discount Drug Mart Vitamin E Hand Sanitizerethyl alcohol	Alcohol 650 mg/mL	LiquidTopical	Discount Drug Mart	53943-022
Freeman Packaging Hand Sanitizeralcohol	Alcohol 62 mL/100mL	LiquidTopical	JIANGMEN SHUIZIRUN SANITARY ARTICLES CO., LTD.	71734-201
Hand Cleanse - Strawberry Pomegranatetriclosan	Triclosan 7.5 mg/500mg	GelTopical	China Ningbo Shangge Cosmetic Technology Corp.	58503-011
Hand Sanitizer	Alcohol .62 mL/mL	GelTopical	LS Promotions Inc.	72449-100
Harris Teeter Spring Fresh Body Washbenzalkonium chloride	Benzalkonium chloride 1.3 mg/mL	LiquidTopical	Harris Teeter	72036-801
Instant Hand Sanitizeralcohol	Alcohol 665 mg/L	GelTopical	Safetec of America, Inc.	61010-5111
Isopropyl Alcoholalcohol	Alcohol 70 mL/100mL	SprayTopical	Zee Medical	35418-402
KidzStuff Hand Sanitizeralcohol	Alcohol 62 g/100g	LiquidTopical	JIANGMEN SHUIZIRUN SANITARY ARTICLES CO., LTD.	71734-204
ONID Wipeethanol	Alcohol 75 mL/100mL	SwabTopical	ONID Technology Corp	71441-180

Antimicrobial Face Body Wash (Benzethonium chloride liquid) NDC 37945-902