menthol 100 MG/ML Topical Spray [Biofreeze]

RxCUI
1043232
RxNorm name
menthol 100 MG/ML Topical Spray [Biofreeze]
Display name
BIOFREEZE (Topical)
Full name
menthol 100 MG/ML Topical Spray [Biofreeze]
Term type
SBD
Status
Active
Strength
10%
Dose form
Spray
Route
Topical
Updated
2026-07-15 00:10:30

RxNorm Status History#

Status
Active
Source
RXNORM
Current
YES
Release start
122010
Active start
122010
Multiple ingredient
NO
Branded
YES

Ingredients And Strength#

Ingredient, Strength, Base table
IngredientStrengthBaseBasis of strength
menthol100 MG / 1 MLmentholmenthol

Dose Form Concepts#

Dose form, RxCUI table
Dose formRxCUI
Topical Spray346165

Derived Ingredient Concepts#

Ingredient, RxCUI table
IngredientRxCUI
menthol6750

Source Vocabulary Codes#

Code type, Values, Count table
Code typeValuesCountCategory
PRESCRIBABLEY1ATTRIBUTES
RXNAV_STRBiofreeze 10 % Topical Spray1NAMES
RxNorm Namementhol 100 MG/ML Topical Spray [Biofreeze]1NAMES
RxNorm Synonym
2 linked values
2NAMES
TTYSBD1ATTRIBUTES
SPL_SET_ID5edddb99-6596-4a3b-b361-1cc04d032c311CODES
RxCUI10432321CODES

FDA NDC Products And Packages#

Package NDC, Product NDC, Name table
Package NDCProduct NDCNameLabelerApplication
59316-104-1059316-104Biofreeze MENTHOLReckitt Benckiser LLCM017
59316-104-2059316-104Biofreeze MENTHOLReckitt Benckiser LLCM017
59316-104-3059316-104Biofreeze MENTHOLReckitt Benckiser LLCM017

Drugs@FDA Applications#

Application, NDC, Name table
ApplicationNDCNameMarketing categoryLabeler
M01759316-104Biofreeze MENTHOLOTC MONOGRAPH DRUGReckitt Benckiser LLC

RxNav Current And Historical NDCs#

RxNav current and historical NDC rows page 1 of 1 · 5 matching rows.

NDC11, Source, Active table
NDC11SourceActive
59316010410rxnav_ndcsyes
59316010420rxnav_ndcsyes
59316010430rxnav_ndcsyes
59316010425rxnav_historical
59316010450rxnav_historical

UNII Substances#

UNII substance links page 1 of 1 · 0 matching rows.

No records found.

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
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
BiofreezeMENTHOLReckitt Benckiser LLC5edddb99-6596-4a3b-b361-1cc04d032c312026-05-13WarningsExact identifier
ndc (package): 59316-104-20
ndc (package): 59316-104-30
ndc (package): 59316-104-10
ndc (product): 59316-104
ndc11 (package): 59316010410
ndc11 (package): 59316010420
ndc11 (package): 59316010430
ndc11 (package): 59316010425
rxcui: 1043232

DailyMed RxNorm Mappings#

unique DailyMed labels mapped to this RxNorm concept page 1 of 1 · 1 matching rows.

Set ID, RxNorm mappings, Terms table
Set IDRxNorm mappingsTermsSPL versionLabelEffective
5edddb99-6596-4a3b-b361-1cc04d032c31BIOFREEZE 10 % Topical Spray [PSN] · menthol 100 MG/ML Topical Spray [Biofreeze] [SBD] · Biofreeze 10 % Topical Spray [SY] · Biofreeze 100 MG/ML Topical Spray [SY]440Biofreeze Pain Relieving Spray20260513

Recently Linked DailyMed Labels#

Set ID, Title, Manufacturer table
Set IDTitleManufacturerEffective
5edddb99-6596-4a3b-b361-1cc04d032c31Biofreeze Pain Relieving SprayReckitt Benckiser LLC | Span Packaging Services LLC dba Multi-Pack Solutions20260513

Drug Classes#

Source, Class ID, Class table
SourceClass IDClassTypeRelationshipDrug concept
MEDRTD008610MentholCHEMhas_ingredientmenthol
MEDRTD004342Drug HypersensitivityDISEASEci_withmenthol
MEDRTD010146PainDISEASEmay_treatmenthol
MEDRTD012871Skin DiseasesDISEASEmay_treatmenthol
MEDRTN0000000069Calcium Channel AntagonistsMOAhas_moamenthol
MEDRTN0000008889Decreased Sensory-Somatic Nervous System Organized Electrical ActivityPEhas_pementhol

Properties#

Category, Property, Value table
CategoryPropertyValue
ATTRIBUTESAVAILABLE_STRENGTH100 MG/ML
ATTRIBUTESGENERAL_CARDINALITYSINGLE
ATTRIBUTESHUMAN_DRUGUS
ATTRIBUTESRXNAV_HUMAN_DRUGUS
NAMESPrescribable SynonymBIOFREEZE 10 % Topical Spray
SOURCESSourceMetathesaurus FDA Structured Product Labels