ZIMS MAX FREEZE

Product NDC
54273-007
11-digit product format
542730007
Labeler code
54273
Product ID
54273-007_3674680c-30ec-49e4-99b2-9319199ff6a5
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
2018-08-01
Substance
MENTHOL, UNSPECIFIED FORM
Active strength
70 mg/g
NDC exclude flag
No
Listing certified through
2026-12-31
Current FDA listing
Yes

openFDA label cross-check#

Cross-check layer: openFDA label JSON enriches search and identifies hydration gaps. The DailyMed Structured Product Label remains the canonical label presentation on FDA.report.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
ZIMS MAX FREEZE PRO FORMULAMENTHOL, UNSPECIFIED FORMKOBAYASHI Healthcare International, Inc.436e8578-b609-4b45-8f84-0d111140fda62023-11-16WarningsExact identifier

Warnings cross-check#

openFDA text is shown for search and cross-checking; DailyMed SPL is canonical.

warnings

Warnings For external use only Rare cases of burns have been reported with products of this type Flammable: Keep away from fire or flame and heated surfaces Do not use if you are allergic to any ingredient in this product on open wounds, damaged or irritated skin with a heating pad or TENS device after expiration date When using this product may cause a burning sensation wherever it is applied, but is usually mild and gradually lessens over time do not bandage tightly do not use otherwise than as directed avoid contact with eyes or mucous membranes Stop use and ask a doctor if burning sensation is painful and persistent condition worsens rash, itching, redness or excessive irritation of the skin develops symptoms persist for more than 7 days symptoms clear up and occur again within a few days If pregnant or breast-feeding, ask a health professional before use. Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

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 Identifiers#

Field, Values table
FieldValues
UniiL7T10EIP3A
Rxcui311509

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
54273-007-01ZIMS MAX FREEZE PRO FORMULA85 g in 1 BOTTLE, WITH APPLICATORGEL858
54273-007-02ZIMS MAX FREEZE PRO FORMULA102 g in 1 BOTTLE, WITH APPLICATORGEL1028

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
54273-007ZIMS MAX FREEZE PRO FORMULA (MENTHOL, UNSPECIFIED FORM) GEL [KOBAYASHI HEALTHCARE INTERNATIONAL, INC.]8Current NDC, Legacy NDC, 2 package rows20231117_436e8578-b609-4b45-8f84-0d111140fda6.zip

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
311509menthol 7 % Topical GelPSN436e8578-b609-4b45-8f84-0d111140fda68
311509menthol 0.07 MG/MG Topical GelSCD436e8578-b609-4b45-8f84-0d111140fda68
311509menthol 7 % Topical GelSY436e8578-b609-4b45-8f84-0d111140fda68

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
54273-007-015427300070185 g in 1 BOTTLE, WITH APPLICATOR (54273-007-01) 85 g2018-08-010000-00-00NoNoCurrent
54273-007-0254273000702102 g in 1 BOTTLE, WITH APPLICATOR (54273-007-02) 102 g2019-02-010000-00-00NoNoCurrent