ZIMS MAX FREEZE

Product NDC
54273-006
11-digit product format
542730006
Labeler code
54273
Product ID
54273-006_85731b59-73da-4aae-adf7-40cff79c4fb3
Type
HUMAN OTC DRUG
Nonproprietary name
MENTHOL, UNSPECIFIED FORM
Dosage form
GEL
Route
TOPICAL
Labeler
KOBAYASHI Healthcare International, Inc.
Application
M017
Marketing category
OTC MONOGRAPH DRUG
Marketing start
2018-07-01
Substance
MENTHOL, UNSPECIFIED FORM
Active strength
70 mg/g
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
ZIMS MAX FREEZE
Brand name suffix
PRO FORMULA
Listing expiration
2026-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
MENTHOL, UNSPECIFIED FORM70 mg/g

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
311509Internal RxNorm lookup

Harmonized SPL set identifiers#

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

Identifier, FDA.report destination table
IdentifierFDA.report destination
b44beac3-1d20-434f-9a79-4fab1ac68791Available on FDA.report

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
54273-006-01ZIMS MAX FREEZE PRO FORMULA113 g in 1 TUBEGEL1137
54273-006-02ZIMS MAX FREEZE PRO FORMULA136 g in 1 TUBEGEL1367
54273-006-03ZIMS MAX FREEZE PRO FORMULA5 g in 1 PACKETGEL57

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
54273-006ZIMS MAX FREEZE PRO FORMULA (MENTHOL, UNSPECIFIED FORM) GEL [KOBAYASHI HEALTHCARE INTERNATIONAL, INC.]7Current NDC, Legacy NDC, 3 package rows20231116_b44beac3-1d20-434f-9a79-4fab1ac68791.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 112 of 152 · 3,029 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
QC Cool and Heat Roll-OnMENTHOL 16%Chain Drug Marketing Association Incd35e9dfa-8a28-fdb3-e053-2995a90abc522024-12-15WarningsExact identifier
application number: M017
Meijer Cold and Hot Pain RelievingMENTHOL 16%Meijerbec62df3-06c9-a115-e053-2995a90a42672024-12-15WarningsExact identifier
application number: M017
Tommie Copper Pain ReliefMENTHOL 16%Tommie Copper, Inc.b4dfa5fa-2d61-db1e-e053-2a95a90a7ac82024-12-15WarningsExact identifier
application number: M017
Pain Relief Liquid RollerCAMPHOR 3.5%, MENTHOL 3.5%Tommie Copper, Inc.c9f0447e-de43-16a5-e053-2995a90a05c12024-12-15WarningsExact identifier
application number: M017
Tommie Copper Pain Relief Maximum StrengthTROLAMINE SALICYLATE 10%Tommie Copper, Inc.b622c14f-9bf3-0bbd-e053-2a95a90a2adc2024-12-15WarningsExact identifier
application number: M017
Copperlife Pain ReliefTROLAMINE SALICYLATE 10%Tommie Copper, Inc.c94d00f9-42ce-1d43-e053-2a95a90a058d2024-12-15WarningsExact identifier
application number: M017
Tommie Copper Pain Relief RollerCAMPHOR 3.5%, MENTHOL 3.5%Tommie Copper, Inc.b6c3d6eb-b485-33b8-e053-2a95a90a41e12024-12-15WarningsExact identifier
application number: M017
Tommie Copper Pain Relief RollerCAMPHOR 3.5%, MENTHOL 3.5%Tommie Copper, Inc.b4cd4fed-e8c8-db85-e053-2995a90a708b2024-12-15WarningsExact identifier
application number: M017
Copperlife Pain Relief LiquidMENTHOL 16%Tommie Copper, Inc.c93a0139-953b-5523-e053-2a95a90a0b2d2024-12-15WarningsExact identifier
application number: M017
Tommie Copper Pain ReliefTROLAMINE SALICYLATE 10%Tommie Copper, Inc.ca011b03-a263-1908-e053-2995a90ad9702024-12-15WarningsExact identifier
application number: M017
Warrior Chiggerex ReliefBENZOCAINE 10%Derma Care Research Labs, LLCdcf2f52b-2295-58e5-e053-2995a90a7fd82024-12-15WarningsExact identifier
application number: M017
Capsaicin CreamCAPSAICINTrifecta Pharmaceuticals USA LLCdef8d341-06a7-0e9b-e053-2995a90a0ad62024-12-13WarningsExact identifier
application number: M017
Mentholatum OriginalCAMPHOR, MENTHOLThe Mentholatum Company19e4b812-67c6-49fd-833a-b432100363f52024-12-13WarningsExact identifier
application number: M017
Cold and Hot MedicatedMENTHOLThe Mentholatum Company85bf425d-59d7-4462-ba46-2921454600992024-12-13WarningsExact identifier
application number: M017
Mentholatum Lidocaine IceLIDOCAINE HCL, MENTHOLThe Mentholatum Company4d74cbab-31cd-4579-9360-6852ee215b5e2024-12-13WarningsExact identifier
application number: M017
Mentholatum Deep Heating Rub Extra StrengthMENTHOL, METHYL SALICYLATEThe Mentholatum Companyf5684158-0d83-4031-b493-5422ddc73e782024-12-13WarningsExact identifier
application number: M017
Discount Drug Mart Anti-ItchCAMPHOR, MENTHOLDiscount Drug Mart87d379da-103a-c751-e053-2995a90a56de2024-12-13WarningsExact identifier
application number: M017
Audiologist Anti-itchHYDROCORTISONEOAKTREE PRODUCTS, INC.853e078e-1e91-d55f-e053-2991aa0a6dcd2024-12-13WarningsExact identifier
application number: M017
CVS Anti itchHYDROCORTISONECVS884df604-711b-4a3d-e053-2995a90a3a042024-12-13WarningsExact identifier
application number: M017
Dermoplast Pain RelievingBENZOCAINE AND LEVOMENTHOLAdvantice Health, LLC2347f0b8-d463-422d-8583-65624d9a1a912024-12-12WarningsExact identifier
application number: M017

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
311509menthol 7 % Topical GelPSNb44beac3-1d20-434f-9a79-4fab1ac687917
311509menthol 0.07 MG/MG Topical GelSCDb44beac3-1d20-434f-9a79-4fab1ac687917
311509menthol 7 % Topical GelSYb44beac3-1d20-434f-9a79-4fab1ac687917

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
54273-006-0154273000601113 g in 1 TUBE (54273-006-01) 113 g2018-07-010000-00-00NoNoCurrent
54273-006-0254273000602136 g in 1 TUBE (54273-006-02) 136 g2019-02-010000-00-00NoNoCurrent
54273-006-03542730006035 g in 1 PACKET (54273-006-03) 5 g2019-01-010000-00-00NoNoCurrent