NeuroSoothe

Product NDC: 85622-510
11-digit product format: 856220510
Labeler code: 85622
Product ID: 85622-510_95e3fdeb-9c7f-4063-b2fe-1597ac453cf4
Type: HUMAN OTC DRUG
Nonproprietary name: Camphor, Menthol
Dosage form: LIQUID
Route: TOPICAL
Labeler: Blue Heron Pharmaceuticals, LLC
Marketing category: UNAPPROVED DRUG OTHER
Marketing start: 2026-02-23
Substance: CAMPHOR (SYNTHETIC); MENTHOL
Active strength: 3; 3 g/85g; g/85g
NDC exclude flag: No
Listing certified through: 2027-12-31
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: NeuroSoothe
Listing expiration: 2027-12-31

Active Ingredients#

Ingredient, Strength table
Ingredient	Strength
CAMPHOR (SYNTHETIC)	3 g/85g
MENTHOL	3 g/85g

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 2 matching rows.

Identifier, FDA.report destination table
Identifier	FDA.report destination
5TJD82A1ET	Internal UNII lookup
L7T10EIP3A	Internal UNII lookup

Harmonized RxCUI identifiers#

RxCUI identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
Identifier	FDA.report destination
630714	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
e3c21cdb-0027-486b-9b83-c1261c3e73a6	Available on FDA.report

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
85622-510-85	NeuroSoothe	85 g in 1 BOTTLE, WITH APPLICATOR	LIQUID	85		1

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDC	Billing unit	Product NDC	DailyMed indexing SPL	SPL version	Effective
85622-510-85	GM - Gram	85622-510	39704397-acd5-42ee-a698-8a0974a90593	1	2026-04-20

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
NeuroSoothe	CAMPHOR, MENTHOL	Blue Heron Pharmaceuticals, LLC	e3c21cdb-0027-486b-9b83-c1261c3e73a6	2026-02-23	Warnings	Exact identifier ndc (product): 85622-510

UNII, Preferred term, Registry number table
UNII	Preferred term	Registry number	Matched term
5TJD82A1ET	CAMPHOR (SYNTHETIC)	76-22-2	CAMPHOR (SYNTHETIC)

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	DailyMed	SPL version
630714	camphor 3 % / menthol 3 % Topical Gel	PSN	e3c21cdb-0027-486b-9b83-c1261c3e73a6	1
630714	camphor 0.03 MG/MG / menthol 0.03 MG/MG Topical Gel	SCD	e3c21cdb-0027-486b-9b83-c1261c3e73a6	1
630714	camphor 3 % / menthol 3 % Topical Gel	SY	e3c21cdb-0027-486b-9b83-c1261c3e73a6	1

Packages#

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Units	Marketing start	Sample	Exclude flag	Status
85622-510-85	85622051085	85 g in 1 BOTTLE, WITH APPLICATOR (85622-510-85)	85 g	2026-02-23	No	No	Current

Title, Manufacturer, Effective date table
Title	Manufacturer	Effective date	Type	Version
NeuroSoothe	Blue Heron Pharmaceuticals, LLC \| SOMBRA COSMETICS INC.	2026-02-23	HUMAN OTC DRUG LABEL	1