AMBI Soothing Hand sanitizer

Product NDC: 73453-143
11-digit product format: 734530143
Labeler code: 73453
Product ID: 73453-143_09751799-664e-ec58-e063-6394a90aea39
Type: HUMAN OTC DRUG
Nonproprietary name: ALCOHOL
Dosage form: GEL
Route: TOPICAL
Labeler: AMBI Enterprises, llc
Application: 505G(a)(3)
Marketing category: OTC MONOGRAPH DRUG
Marketing start: 2020-05-20
Substance: ALCOHOL
Active strength: .7 mL/mL
NDC exclude flag: No
Listing certified through: 2026-12-31
Current FDA listing: Yes

Additional Listing Data#

Finished product: Yes
Brand name base: AMBI Soothing Hand sanitizer
Listing expiration: 2026-12-31

Active Ingredients#

Ingredient, Strength table
Ingredient	Strength
ALCOHOL	.7 mL/mL

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
581662	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
229a2afd-9f33-42b9-916d-df1e787181f7	Available on FDA.report

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
73453-143-04	AMBI Soothing Hand sanitizer	118 mL in 1 CYLINDER	GEL	118		2

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
73453-143	AMBI SOOTHING HAND SANITIZER (ALCOHOL) GEL [AMBI ENTERPRISES, LLC]	2	Current NDC, Legacy NDC, 1 package rows	20231106_229a2afd-9f33-42b9-916d-df1e787181f7.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
AMBI Soothing Hand sanitizer	ALCOHOL	AMBI Enterprises, llc	229a2afd-9f33-42b9-916d-df1e787181f7	2023-11-05	Warnings	Exact identifier ndc (product): 73453-143

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
581662	ethanol 70 % Topical Gel	PSN	229a2afd-9f33-42b9-916d-df1e787181f7	2
581662	ethanol 0.7 ML/ML Topical Gel	SCD	229a2afd-9f33-42b9-916d-df1e787181f7	2
581662	ethanol 70 % Topical Gel	SY	229a2afd-9f33-42b9-916d-df1e787181f7	2
581662	ethyl alcohol 70 % Topical Gel	SY	229a2afd-9f33-42b9-916d-df1e787181f7	2

Packages#

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Units	Marketing start	Marketing end	Sample	Exclude flag	Status
73453-143-04	73453014304	118 mL in 1 CYLINDER (73453-143-04)	118 ml	2020-05-20	0000-00-00	No	No	Current