Anti Bacterial Hand Gel

Product NDC: 62670-6737
Requested package NDC: 62670-6737-0
11-digit product format: 626706737
Labeler code: 62670
Product ID: 62670-6737_29a5342a-e6dd-ea55-e063-6394a90a11e8
Type: HUMAN OTC DRUG
Nonproprietary name: Alcohol
Dosage form: GEL
Route: TOPICAL
Labeler: Bath & Body Works, Inc.
Application: 505G(a)(3)
Marketing category: OTC MONOGRAPH DRUG
Marketing start: 2024-07-29
Marketing end: 2027-07-29
Substance: ALCOHOL
Active strength: 71 mL/100mL
NDC exclude flag: No
Current FDA listing: Yes

Additional Listing Data#

Finished product: Yes
Brand name base: Anti Bacterial Hand Gel
Brand name suffix: Flannel

Active Ingredients#

Ingredient, Strength table
Ingredient	Strength
ALCOHOL	71 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
2282911	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
29a54361-e108-20d7-e063-6294a90a117a	Available on FDA.report

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
62670-6737-0	Anti Bacterial Hand GelFlannel	29 mL in 1 BOTTLE	GEL	29		1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
62670-6737	ANTI BACTERIAL HAND GEL FLANNEL (ALCOHOL) GEL [BATH & BODY WORKS, INC.]	1	Current NDC, 1 package rows	20241222_29a54361-e108-20d7-e063-6294a90a117a.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
Anti Bacterial Hand Gel Flannel	ALCOHOL	Bath & Body Works, Inc.	29a54361-e108-20d7-e063-6294a90a117a	2024-12-19	Warnings	Exact identifier ndc (package): 62670-6737-0 ndc (product): 62670-6737 ndc11 (package): 62670673700

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
2282911	ethanol 71 % Topical Gel	PSN	29a54361-e108-20d7-e063-6294a90a117a	1
2282911	ethanol 0.71 ML/ML Topical Gel	SCD	29a54361-e108-20d7-e063-6294a90a117a	1
2282911	ethanol 71 % Topical Gel	SY	29a54361-e108-20d7-e063-6294a90a117a	1

Packages#

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Units	Marketing start	Marketing end	Sample	Exclude flag	Status
62670-6737-0	62670673700	29 mL in 1 BOTTLE (62670-6737-0)	29 ml	2024-07-29	2027-07-29	No	No	Historical

Title, Manufacturer, Effective date table
Title	Manufacturer	Effective date	Type	Version
ABHG Flannel	Bath & Body Works, Inc. \| KDC US Holdings, Inc. \| Memphis Contract Packaging	2024-12-19	HUMAN OTC DRUG LABEL	1