FDA.reportPublic FDA data

ICY FREEZE

Product NDC
66902-165
11-digit product format
669020165
Labeler code
66902
Product ID
66902-165_a6e37537-90e9-4edd-9a7c-cf0b91deba1c
Type
HUMAN OTC DRUG
Nonproprietary name
MENTHOL
Dosage form
GEL
Route
TOPICAL
Labeler
NATURAL ESSENTIALS, INC.
Application
part348
Marketing category
OTC MONOGRAPH NOT FINAL
Marketing start
2017-12-01
Substance
MENTHOL
Active strength
35 mg/mL
NDC exclude flag
No
Listing certified through
2026-12-31
Current FDA listing
Yes

Additional Listing Data#

Finished product
Yes
Brand name base
ICY FREEZE
Listing expiration
2026-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
MENTHOL35 mg/mL

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
L7T10EIP3AInternal UNII lookup

Harmonized RxCUI identifiers#

RxCUI identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
808955Internal RxNorm lookup

Harmonized SPL set identifiers#

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

Identifier, FDA.report destination table
IdentifierFDA.report destination
41b2e9a0-818d-4188-8c9d-8ff7c0d0519bAvailable 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
66902-165-03ICY FREEZE90 mL in 1 BOTTLEGEL901
66902-165-03ICY FREEZE1 in 1 BOTTLE, WITH APPLICATORGEL11
66902-165-04ICY FREEZE1 in 1 BOTTLE, PUMPGEL11
66902-165-04ICY FREEZE120 mL in 1 BOTTLEGEL1201

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
66902-165ICY FREEZE (MENTHOL) GEL [NATURAL ESSENTIALS, INC.]1Current NDC, Legacy NDC, 4 package rows20171201_41b2e9a0-818d-4188-8c9d-8ff7c0d0519b.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
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
ICY FREEZEMENTHOLNATURAL ESSENTIALS, INC.41b2e9a0-818d-4188-8c9d-8ff7c0d0519b2017-12-01WarningsExact identifier
ndc (product): 66902-165

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
808955menthol 3.5 % Topical GelPSN41b2e9a0-818d-4188-8c9d-8ff7c0d0519b1
808955menthol 0.035 MG/MG Topical GelSCD41b2e9a0-818d-4188-8c9d-8ff7c0d0519b1
808955menthol 3.5 % Topical GelSY41b2e9a0-818d-4188-8c9d-8ff7c0d0519b1

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
66902-165-03669020165031 BOTTLE in 1 BOTTLE, WITH APPLICATOR (66902-165-03) / 90 mL in 1 BOTTLE1 bottle2017-12-010000-00-00NoNoCurrent
66902-165-04669020165041 BOTTLE in 1 BOTTLE, PUMP (66902-165-04) / 120 mL in 1 BOTTLE1 bottle2017-12-010000-00-00NoNoCurrent