Yeheal

Product NDC
87008-813
11-digit product format
870080813
Labeler code
87008
Product ID
87008-813_3cf1bc74-3061-6d63-e063-6294a90a9f5c
Type
HUMAN OTC DRUG
Nonproprietary name
Camphor, Menthol, Isopropyl Alcohol
Dosage form
SPRAY
Route
TOPICAL
Labeler
Shenzhen Yeheal Biotechnology Co., Ltd
Application
M017
Marketing category
OTC MONOGRAPH DRUG
Marketing start
2025-08-13
Substance
CAMPHOR, (-)-; MENTHOL; ISOPROPYL ALCOHOL
Active strength
2; 2; 75 mg/100mg; mg/100mg; mg/100mg
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
Yeheal
Listing expiration
2026-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
CAMPHOR, (-)-2 mg/100mg
MENTHOL2 mg/100mg
ISOPROPYL ALCOHOL75 mg/100mg

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 3 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
213N3S8275Internal UNII lookup
L7T10EIP3AInternal UNII lookup
ND2M416302Internal UNII lookup

Harmonized SPL set identifiers#

SPL set identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
3cf1bc74-3060-6d63-e063-6294a90a9f5cAvailable on FDA.report

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
6c13b22c-b3ba-4127-b768-0132dd5ab0d1Product name120230829

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
87008-813-01Yeheal90 mg in 1 BOTTLE, SPRAYSPRAY901
87008-813-02Yeheal1 in 1 BOXSPRAY11

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 48 of 153 · 3,057 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
Nufabrx Elbow SleeveCAPSAICINNufabrx LLC473004cd-f7f9-3c68-e063-6294a90a5b8a2025-12-30WarningsExact identifier
application number: M017
Nufabrx Leg SleeveCAPSAICINNufabrx LLC473015ed-3e0f-6eae-e063-6294a90a4c742025-12-30WarningsExact identifier
application number: M017
Nufabrx Arm SleeveCAPSAICINNufabrx LLC472ef560-1ed6-c912-e063-6394a90aaa1c2025-12-30WarningsExact identifier
application number: M017
Nufabrx Shin SleeveCAPSAICINNufabrx LLC4730bf64-ea0c-ca8d-e063-6394a90af5422025-12-30WarningsExact identifier
application number: M017
Nufabrx Ankle SleeveCAPSAICINNufabrx LLC4730d164-9027-fff2-e063-6394a90a42802025-12-30WarningsExact identifier
application number: M017
Nufabrx Knee SleeveCAPSAICINNufabrx LLC473098ca-02f1-c287-e063-6394a90a37e12025-12-30WarningsExact identifier
application number: M017
PAIN RELIEF PATCHESLIDOCAINELiberty Procurement, In2d381c48-402f-4e46-81b2-41a184139a612025-12-30WarningsExact identifier
application number: M017
Thera Care Pain Relief Menthol PatchsMENTHOLVeridian Healthcare1faa1d4f-b7fb-4f36-aef1-2fedde114b8e2025-12-30WarningsExact identifier
application number: M017
Lidocaine Pain ReliefLIDOCAINE PAIN RELIEFAllegiant Health7f715144-f0c8-48fc-a22d-eac85759c66a2025-12-30WarningsExact identifier
application number: M017
ZIKS ARTHRITIS PAIN RELIEFZIKS ARTHRITIS PAIN RELIEFNnodum Pharmaceuticals5dd4fefc-b70a-4850-819c-1cca6f28aa972025-12-29WarningsExact identifier
application number: M017
Ted and Gregs Pain Rub with Resveratrol Topical AnalgesicMETHYL SALICYLATETed and Greg's Inc.c699438d-595d-4711-801b-51e960aa36682025-12-29WarningsExact identifier
application number: M017
Frankincense and Myrrh Arthritis Pain Combo PackMENTHOLWISE CONSUMER PRODUCTS CO.47199677-e04c-768b-e063-6294a90a35242025-12-29WarningsExact identifier
application number: M017
Witch HazelWITCH HAZELCVS HEALTHb8b79e8d-9c84-1700-e053-2995a90af5bd2025-12-29WarningsExact identifier
application number: M017
WALGREENS BURNLIDOCAINE HYDROCHLORIDEWALGREENSb61e6d73-4f41-ef50-e053-2a95a90a0fc62025-12-29WarningsExact identifier
application number: M017
CVS cold and HotMENTHOL 16%CVSd1676df9-530f-1664-e053-2995a90a5b642025-12-29WarningsExact identifier
application number: M017
HydrocortisoneHYDROCORTISONEAKRON PHARMA INCfa956b6a-1712-4f7a-9490-11866dcd17c82025-12-29WarningsExact identifier
application number: M017
Frankincense and Myrrh Nerve Combo PackMENTHOLWise Consumer Products471d815c-1c34-e0f8-e063-6294a90aca782025-12-29WarningsExact identifier
application number: M017
Pain ReleaseMENTHOLNatures Formulae Health Products Ltd.781d3c8d-7b70-e973-e053-2991aa0aaa782025-12-29WarningsExact identifier
application number: M017
Pain ReleaseMENTHOLNatures Formulae Health Products Ltd.781dfd66-f006-a2d7-e053-2991aa0a170c2025-12-29WarningsExact identifier
application number: M017
Pain ReleaseMENTHOLNatures Formulae Health Products Ltd.781d53cf-b3df-3e2b-e053-2a91aa0a7dcd2025-12-29WarningsExact identifier
application number: M017

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startSampleExclude flagStatus
87008-813-018700808130190 mg in 1 BOTTLE, SPRAY90 mgHistorical
87008-813-02870080813021 BOTTLE, SPRAY in 1 BOX (87008-813-02) / 90 mg in 1 BOTTLE, SPRAY (87008-813-01) 2025-08-13NoNoCurrent