AFCO 5508 Sanifect Foam-E II

Product NDC: 66949-139
11-digit product format: 669490139
Labeler code: 66949
Product ID: 66949-139_46dfe3ae-bb1d-7a50-e063-6394a90a96c7
Type: HUMAN OTC DRUG
Nonproprietary name: Ethanol
Dosage form: LIQUID
Route: TOPICAL
Labeler: Zep Inc.
Application: 505G(a)(3)
Marketing category: OTC MONOGRAPH DRUG
Marketing start: 2025-05-05
Marketing end: 2026-12-31
Substance: CHLOROXYLENOL
Active strength: 2081980 mg/208198mL
NDC exclude flag: No
Current FDA listing: Yes

Additional Listing Data#

Finished product: Yes
Brand name base: AFCO 5508 Sanifect Foam-E II

Active Ingredients#

Ingredient, Strength table
Ingredient	Strength
CHLOROXYLENOL	2081980 mg/208198mL

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
Identifier	FDA.report destination
0F32U78V2Q	Internal UNII lookup

Harmonized RxCUI identifiers#

RxCUI identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
Identifier	FDA.report destination
413257	Internal RxNorm lookup

Harmonized SPL set identifiers#

SPL set identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
Identifier	FDA.report destination
347995ef-38bd-7cdb-e063-6394a90adec3	Available on FDA.report

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	SPL version
66949-139-01	AFCO 5508 Sanifect Foam-E II	208198 mL in 1 DRUM	LIQUID	208198	2
66949-139-02	AFCO 5508 Sanifect Foam-E II	6000 mL in 1 CASE	LIQUID	6000	2
66949-139-03	AFCO 5508 Sanifect Foam-E II	3785 mL in 1 CASE	LIQUID	3785	2

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
66949-139	AFCO 5508 SANIFECT FOAM-E II (ETHANOL) LIQUID [ZEP INC.]	1	Current NDC, 3 package rows	20250515_347995ef-38bd-7cdb-e063-6394a90adec3.zip

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
AFCO 5508 Sanifect Foam-E II	ETHANOL	Zep Inc.	347995ef-38bd-7cdb-e063-6394a90adec3	2025-12-26	Warnings	Exact identifier ndc (product): 66949-139

UNII, Preferred term, Registry number table
UNII	Preferred term	Registry number	Matched term
0F32U78V2Q	CHLOROXYLENOL	88-04-0	CHLOROXYLENOL

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	DailyMed	SPL version
413257	chloroxylenol 1 % Medicated Liquid Soap	PSN	347995ef-38bd-7cdb-e063-6394a90adec3	2
413257	chloroxylenol 10 MG/ML Medicated Liquid Soap	SCD	347995ef-38bd-7cdb-e063-6394a90adec3	2
413257	chloroxylenol 1 % Medicated Liquid Soap	SY	347995ef-38bd-7cdb-e063-6394a90adec3	2

Packages#

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Units	Marketing start	Marketing end	Sample	Exclude flag	Status
66949-139-01	66949013901	208198 mL in 1 DRUM (66949-139-01)	208198 ml	2025-05-05	2026-12-31	No	No	Historical
66949-139-02	66949013902	6000 mL in 1 CASE (66949-139-02)	6000 ml	2025-05-05	2026-12-31	No	No	Historical
66949-139-03	66949013903	3785 mL in 1 CASE (66949-139-03)	3785 ml	2025-05-05	2026-12-31	No	No	Historical