NDC codes

FDA NDC Directory
Product NDC (as listed)66949-140Labeler and product segments. Claims need a package NDC.
Product NDC at billing width66949-0140Add 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
66949-140-0166949014001208198 mL in 1 DRUM (66949-140-01)Marketed from May 5, 2025
66949-140-02669490140026000 mL in 1 CASE (66949-140-02)Marketed from May 5, 2025
66949-140-03669490140033785 mL in 1 CASE (66949-140-03)Marketed from May 5, 2025

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)
AFCO 5511 Sanifect E3
Generic name (nonproprietary)
ethanol
Active ingredients
Alcohol — 70 mL/100mL
Dosage form
Liquid
Route
Topical
Labeler
Zep Inc.NDC labeler code 66949
Product type
Over-the-counter drug
Marketing category
OTC monograph drugApplication 505G(a)(3)
Marketing start
Listing expires
Identifiers
Product ID 66949-140_58f0e6d7-7846-bcdc-e063-6394a90af1b9SPL ID 58f0e6d7-7846-bcdc-e063-6394a90af1b9SPL set ID 34795eba-9ec4-6401-e063-6394a90af428RxCUI 1041849UNII 3K9958V90M

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

N466949014001 followed by a unit qualifier and the quantity

Package 66949-0140-01. 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)

Uses Hand sanitizing to decrease bacteria on skin. No rinsing required.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 66949-140

What is NDC 66949-140?
66949-140 is the product NDC for AFCO 5511 Sanifect E3 (ethanol), Alcohol 70 mL/100mL liquid, listed with the FDA by Zep Inc.. It has 3 package NDCs, shown above in 10- and 11-digit form.
What drug is associated with this NDC?
AFCO 5511 Sanifect E3 (Ethanol).
What is the active ingredient?
Alcohol.
Who is the labeler?
Zep Inc., NDC labeler code 66949. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for AFCO 5511 Sanifect E3?
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)
ProductStrengthForm · routeLabelerProduct NDC
Aura Lane Hand Sanitizer Cherry Blossom Scentethyl alcoholAlcohol 70 mL/100mLSprayTopicalDiamond Life Cosmetics Trading FZCO87247-459
TAGOQHIA Minoxidil Hair Thickening SerumminoxidilMinoxidil 5 g/100mL; Biotin .2 g/100mLLiquidTopicalGuangzhou Borderless Technology Co., Ltd.85304-030
TriDerma Pressure Sore Relieftriderma pressure sore relief wound cleanserBenzethonium chloride .0012 g/gLiquidTopicalGenuine Virgin Aloe Corporation10738-031
Antispeticeucalyptol, menthol, methyl salicylate, thymolEucalyptol .92 mg/mL + 3 more ingredientsMouthwashOralBetter Living Brands, LLC21130-072
PURELL Hand Sanitizer SP Rosewater and LotusalcoholAlcohol 85 mL/100mLSprayTopicalGOJO Industries, LLC21749-994
Ashley Belle Moisturizing Hand Sanitizer Sunset AmberalcoholAlcohol 70 mL/100mLSprayTopicalMy Imports Usa, LLC51628-0041
North Woods Derma Foam E-2benzalkonium chlorideBenzalkonium chloride 1.3 mg/mLSoapTopicalSuperior Chemical Corporation53125-817
laxativebisacodylBisacodyl 5 mg/1Tablet, Delayed releaseOralPublix Super Markets Inc56062-327
Anti Bacterial Hand Gel Winter Candy ApplealcoholAlcohol 71 mL/100mLGelTopicalBath & Body Works, Inc.62670-6755
Anti Bacterial Hand Gel Disney Princess TianaalcoholAlcohol 71 mL/100mLGelTopicalBath & Body Works, Inc.62670-7015
Instant Hand Sanitizer Wipesalcohol hand sanitizer wipesAlcohol 70 mL/100mLClothTopicalDiamond Wipes International, Inc.64709-185
Natural Extensions Fragrance- Free Instant Hand SanitizeralcoholAlcohol 60 mL/100mLGelTopicalBenco Dental66975-101
Walgreenbenzalkonium chlorideBenzalkonium chloride 130 mg/100mLSoapTopicalWalgreen Co0363-0242
Antispeticeucalyptol, menthol, methyl salicylate, thymolEucalyptol .92 mg/mL + 3 more ingredientsMouthwashOralADUSA Distribution, LLC72476-664
Advanced Hand Sanitizerethyl alcoholAlcohol 70 mL/100mLGelTopicalWalmart Inc.79903-334
Alcohol padsIsopropyl alcohol 70 mL/100mLPatchTopicalSHENZHEN BENLIJU BIO-TECH CO.,LTD84449-001
Sour Lemon Hand Sanitizer Fresh Watermelon Scentethyl alcoholAlcohol 70 mL/100mLSprayTopicalDiamond Life Cosmetics Trading FZCO87247-456
5% MINOXIDIL HAIR REGROWTH SERUM With BiotinminoxidilMinoxidil 5 g/100mL; Biotin .2 g/100mLLiquidTopicalGuangzhou Borderless Technology Co., Ltd.85304-027
stimulant laxative enteric coatedbisacodylBisacodyl 5 mg/1TabletOralSportpharm LLC85766-148
PVP Iodine Prep Pad Medium and Largeprovidone iodinePovidone-iodine 10 mg/mLSwabTopicalProfessional Disposables International, Inc.10819-3883

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