FDA.reportPublic FDA data

AFCO 5508 Sanifect Foam-E II

Product NDC
66949-141
11-digit product format
669490141
Labeler code
66949
Product ID
66949-141_46deac6a-c618-0da2-e063-6394a90a02c2
Type
HUMAN OTC DRUG
Nonproprietary name
Chloroxylenol
Dosage form
LIQUID
Route
TOPICAL
Labeler
Zep Inc.
Application
505G(a)(3)
Marketing category
OTC MONOGRAPH DRUG
Marketing start
2025-10-23
Substance
CHLOROXYLENOL
Active strength
2081980 mg/208198mL
NDC exclude flag
No
Listing certified through
2026-12-31
Current FDA listing
Yes

Additional Listing Data#

Finished product
Yes
Brand name base
AFCO 5508 Sanifect Foam-E II
Listing expiration
2026-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
CHLOROXYLENOL2081980 mg/208198mL

Harmonized Identifiers#

Field, Values table
FieldValues
Unii0F32U78V2Q
Rxcui413257

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
66949-141-01AFCO 5508 Sanifect Foam-E II208198 mL in 1 DRUMLIQUID2081981
66949-141-02AFCO 5508 Sanifect Foam-E II6000 mL in 1 CASELIQUID60001
66949-141-03AFCO 5508 Sanifect Foam-E II3785 mL in 1 CASELIQUID37851

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
413257chloroxylenol 1 % Medicated Liquid SoapPSN46deac5c-97e8-8924-e063-6294a90a5dbc1
413257chloroxylenol 10 MG/ML Medicated Liquid SoapSCD46deac5c-97e8-8924-e063-6294a90a5dbc1
413257chloroxylenol 1 % Medicated Liquid SoapSY46deac5c-97e8-8924-e063-6294a90a5dbc1

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startSampleExclude flagStatus
66949-141-0166949014101208198 mL in 1 DRUM (66949-141-01) 208198 ml2025-10-23NoNoCurrent
66949-141-02669490141026000 mL in 1 CASE (66949-141-02) 6000 ml2025-10-23NoNoCurrent
66949-141-03669490141033785 mL in 1 CASE (66949-141-03) 3785 ml2025-10-23NoNoCurrent