NDC 10742-3004

Mentholatum Natural Ice Original

Dimethicone, Octinoxate, Octisalate

Mentholatum Natural Ice Original is a Topical Ointment in the Human Otc Drug category. It is labeled and distributed by The Mentholatum Company. The primary component is Dimethicone; Octinoxate; Octisalate.

Product ID10742-3004_24cc4906-53dd-495d-8d02-f6ea8b6b584f
NDC10742-3004
Product TypeHuman Otc Drug
Proprietary NameMentholatum Natural Ice Original
Generic NameDimethicone, Octinoxate, Octisalate
Dosage FormOintment
Route of AdministrationTOPICAL
Marketing Start Date1999-01-19
Marketing CategoryOTC MONOGRAPH NOT FINAL / OTC MONOGRAPH NOT FINAL
Application Numberpart352
Labeler NameThe Mentholatum Company
Substance NameDIMETHICONE; OCTINOXATE; OCTISALATE
Active Ingredient Strength10 mg/g; mg/g; mg/g
NDC Exclude FlagN
Listing Certified Through2022-12-31

Packaging

NDC 10742-3004-2

1 TUBE in 1 BLISTER PACK (10742-3004-2) > 4.2 g in 1 TUBE
Marketing Start Date2019-04-02
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 10742-3004-2 [10742300402]

Mentholatum Natural Ice Original OINTMENT
Marketing CategoryOTC monograph not final
Application Numberpart352
Product TypeHUMAN OTC DRUG
Marketing Start Date2019-04-02

NDC 10742-3004-5 [10742300405]

Mentholatum Natural Ice Original OINTMENT
Marketing CategoryOTC monograph not final
Application Numberpart352
Product TypeHUMAN OTC DRUG
Marketing Start Date1999-01-19
Marketing End Date2014-10-08

NDC 10742-3004-9 [10742300409]

Mentholatum Natural Ice Original OINTMENT
Marketing CategoryOTC monograph not final
Application Numberpart352
Product TypeHUMAN OTC DRUG
Marketing Start Date1999-01-19
Marketing End Date2019-04-01

NDC 10742-3004-3 [10742300403]

Mentholatum Natural Ice Original OINTMENT
Marketing CategoryOTC monograph not final
Application Numberpart352
Product TypeHUMAN OTC DRUG
Marketing Start Date1999-01-19

NDC 10742-3004-4 [10742300404]

Mentholatum Natural Ice Original OINTMENT
Marketing CategoryOTC monograph not final
Application Numberpart352
Product TypeHUMAN OTC DRUG
Marketing Start Date1999-01-19

NDC 10742-3004-1 [10742300401]

Mentholatum Natural Ice Original OINTMENT
Marketing CategoryOTC monograph not final
Application Numberpart352
Product TypeHUMAN OTC DRUG
Marketing Start Date1999-01-19
Marketing End Date2019-04-01

NDC 10742-3004-8 [10742300408]

Mentholatum Natural Ice Original OINTMENT
Marketing CategoryOTC monograph not final
Application Numberpart352
Product TypeHUMAN OTC DRUG
Marketing Start Date2019-04-02

Drug Details

Active Ingredients

IngredientStrength
DIMETHICONE10 mg/g

OpenFDA Data

SPL SET ID:29220eaa-87cb-4ebe-87db-d36288b3a9e4
Manufacturer
UNII

NDC Crossover Matching brand name "Mentholatum Natural Ice Original" or generic name "Dimethicone, Octinoxate, Octisalate"

NDCBrand NameGeneric Name
10742-8865Mentholatum Medicated Lip Balmdimethicone, octinoxate, octisalate
10742-8893Mentholatum Medicated Lip Balmdimethicone, octinoxate, octisalate
10742-1048Mentholatum Natural Icedimethicone, octinoxate, octisalate
10742-3004Mentholatum Natural Icedimethicone, octinoxate, octisalate

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