SANMO-BL

openFDA label record#

This page contains supplementary openFDA label data. For the canonical label presentation, use the corresponding DailyMed Structured Product Label.

Verified complete openFDA source JSON (canonical bytes are SHA-256 checked before publication)

Brand name: SANMO-BL
Generic name: MOISTURIZING SANITIZER WITH BLUE BEADS
Manufacturer: Beacon Promotions, Inc.
Product type: HUMAN OTC DRUG
SPL set ID: 1eb96fb8-d750-9241-e063-6394a90a1cdd
SPL ID: 48390ab4-8575-bac5-e063-6394a90ae1e4
Version: 2
Effective date: 2026-01-12
Source export date: 2026-09-28
Source partition: 10
Source file: https://download.open.fda.gov/drug/label/drug-label-0010-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-09-28/4bbc9760f647649b787710953d978bd6419e899ba8b90f32c3d972aae43947f8/drug-label-0010-of-0014.json.zip
Source manifest SHA-256: cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run: 20260929T050834Z
Imported at: 2026-09-29 06:05:58

Harmonized routes table
Harmonized routes
TOPICAL

Harmonized identifier links#

Every typed identifier imported from the complete openFDA harmonization object is paginated here; values are not reduced to a first match.

Harmonized identifiers page 1 of 1 · 27 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
application number		M003	openfda.application_number
brand name		SANMO-BL	openfda.brand_name
generic name		MOISTURIZING SANITIZER WITH BLUE BEADS	openfda.generic_name
manufacturer name		Beacon Promotions, Inc.	openfda.manufacturer_name
ndc	package	70445-607-05	openfda.package_ndc
ndc	package	70445-607-08	openfda.package_ndc
ndc	package	70445-607-02	openfda.package_ndc
ndc	package	70445-607-04	openfda.package_ndc
ndc	package	70445-607-09	openfda.package_ndc
ndc	package	70445-607-07	openfda.package_ndc
ndc	package	70445-607-03	openfda.package_ndc
ndc	package	70445-607-06	openfda.package_ndc
ndc	package	70445-607-01	openfda.package_ndc
ndc	product	70445-607	openfda.product_ndc
ndc11	package	70445060706	derived:openfda.package_ndc
ndc11	package	70445060709	derived:openfda.package_ndc
ndc11	package	70445060707	derived:openfda.package_ndc
ndc11	package	70445060704	derived:openfda.package_ndc
ndc11	package	70445060702	derived:openfda.package_ndc
ndc11	package	70445060703	derived:openfda.package_ndc
ndc11	package	70445060701	derived:openfda.package_ndc
ndc11	package	70445060708	derived:openfda.package_ndc
ndc11	package	70445060705	derived:openfda.package_ndc
rxcui		2003712	openfda.rxcui
spl id		48390ab4-8575-bac5-e063-6394a90ae1e4	id
spl set id		1eb96fb8-d750-9241-e063-6394a90a1cdd	set_id
unii		3K9958V90M	openfda.unii

Warnings cross-check#

openFDA text is shown for search and cross-checking; DailyMed SPL is canonical.

Warnings sections page 1 of 1 · 1 matching rows.

warnings

Warnings Warnings Flammable. Keep away from fire or flame. ■ For external use only. ■ When using this product do not use in or near the eyes. In case of contact, rinse eyes thoroughly with water. ■ Stop use and ask a doctor if irritation or rash appears and lasts. ■ Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away. Keep Out Of Reach Of Children Keep out of reach of children

Reported adverse events (FAERS/openFDA)#

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