Hand Sanitizer Foam

Product NDC: 77955-002
11-digit product format: 779550002
Labeler code: 77955
Product ID: 77955-002_0f8c7c79-62a8-3513-e063-6294a90a16df
Type: HUMAN OTC DRUG
Nonproprietary name: Alcohol
Dosage form: SOLUTION
Route: TOPICAL
Labeler: Custom Chemical Solutions
Application: 505G(a)(3)
Marketing category: OTC MONOGRAPH DRUG
Marketing start: 2020-10-05
Substance: ALCOHOL
Active strength: 70 mL/100mL
NDC exclude flag: No
Listing certified through: 2026-12-31
Current FDA listing: Yes

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.

Additional Listing Data#

Finished product: Yes
Brand name base: Hand Sanitizer Foam
Listing expiration: 2026-12-31

Active Ingredients#

Ingredient, Strength table
Ingredient	Strength
ALCOHOL	70 mL/100mL

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
Identifier	FDA.report destination
3K9958V90M	Internal UNII lookup

Harmonized RxCUI identifiers#

RxCUI identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
Identifier	FDA.report destination
616805	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
b0f1cb6f-0b47-7652-e053-2a95a90a7c6b	Available on FDA.report

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
77955-002-02	Hand Sanitizer Foam	1000 mL in 1 BOTTLE	SOLUTION	1000		2

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
77955-002	HAND SANITIZER FOAM (ALCOHOL) SOLUTION [CUSTOM CHEMICAL SOLUTIONS]	2	Current NDC, Legacy NDC, 1 package rows	20240123_b0f1cb6f-0b47-7652-e053-2a95a90a7c6b.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
Hand Sanitizer Foam	ALCOHOL	Custom Chemical Solutions	b0f1cb6f-0b47-7652-e053-2a95a90a7c6b	2024-01-22	Warnings	Exact identifier ndc (product): 77955-002

UNII, Preferred term, Registry number table
UNII	Preferred term	Registry number	Matched term
3K9958V90M	ALCOHOL	64-17-5	ALCOHOL

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	DailyMed	SPL version
616805	ethanol 70 % Topical Foam	PSN	b0f1cb6f-0b47-7652-e053-2a95a90a7c6b	2
616805	ethanol 0.7 ML/ML Topical Foam	SCD	b0f1cb6f-0b47-7652-e053-2a95a90a7c6b	2
616805	ethanol 70 % Topical Foam	SY	b0f1cb6f-0b47-7652-e053-2a95a90a7c6b	2

Packages#

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Units	Marketing start	Marketing end	Sample	Exclude flag	Status
77955-002-02	77955000202	1000 mL in 1 BOTTLE (77955-002-02)	1000 ml	2020-10-05	0000-00-00	No	No	Current