NDC 52000-013

Ice Cold Analgesic Gel

Menthol And Camphor

Ice Cold Analgesic Gel is a Topical Gel in the Human Otc Drug category. It is labeled and distributed by Universal Distribution Center Llc. The primary component is Menthol; Camphor (synthetic).

Product ID52000-013_149e60fd-1d2b-498e-9164-b37d82d91e5b
NDC52000-013
Product TypeHuman Otc Drug
Proprietary NameIce Cold Analgesic Gel
Generic NameMenthol And Camphor
Dosage FormGel
Route of AdministrationTOPICAL
Marketing Start Date2013-03-15
Marketing CategoryOTC MONOGRAPH FINAL / OTC MONOGRAPH FINAL
Application Numberpart341
Labeler NameUniversal Distribution Center LLC
Substance NameMENTHOL; CAMPHOR (SYNTHETIC)
Active Ingredient Strength1 g/100g; g/100g
NDC Exclude FlagN
Listing Certified Through2019-12-31

Packaging

NDC 52000-013-13

170 g in 1 BOTTLE, PLASTIC (52000-013-13)
Marketing Start Date2022-02-14
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 52000-013-16 [52000001316]

Ice Cold Analgesic Gel GEL
Marketing CategoryOTC monograph final
Application Numberpart341
Product TypeHUMAN OTC DRUG
Marketing Start Date2013-03-15
Inactivation Date2020-01-31

NDC 52000-013-18 [52000001318]

Ice Cold Analgesic Gel GEL
Marketing CategoryOTC monograph final
Application Numberpart341
Product TypeHUMAN OTC DRUG
Marketing Start Date2013-03-15
Inactivation Date2020-01-31

NDC 52000-013-13 [52000001313]

Ice Cold Analgesic Gel GEL
Marketing CategoryOTC monograph final
Application Numberpart341
Product TypeHUMAN OTC DRUG
Marketing Start Date2013-03-15
Inactivation Date2020-01-31

NDC 52000-013-14 [52000001314]

Ice Cold Analgesic Gel GEL
Marketing CategoryOTC monograph final
Application Numberpart341
Product TypeHUMAN OTC DRUG
Marketing Start Date2013-03-15
Inactivation Date2020-01-31

NDC 52000-013-15 [52000001315]

Ice Cold Analgesic Gel GEL
Marketing CategoryOTC monograph final
Application Numberpart341
Product TypeHUMAN OTC DRUG
Marketing Start Date2013-03-15
Inactivation Date2020-01-31

NDC 52000-013-17 [52000001317]

Ice Cold Analgesic Gel GEL
Marketing CategoryOTC monograph final
Application Numberpart341
Product TypeHUMAN OTC DRUG
Marketing Start Date2013-03-15
Inactivation Date2020-01-31

Drug Details

Active Ingredients

IngredientStrength
MENTHOL1 g/100g

OpenFDA Data

SPL SET ID:422bd4a3-f03f-496e-b44f-d51885678baa
Manufacturer
UNII
RxNorm Concept Unique ID - RxCUI
  • 1043046
  • UPC Code
  • 0676979248400
  • NDC Crossover Matching brand name "Ice Cold Analgesic Gel" or generic name "Menthol And Camphor"

    NDCBrand NameGeneric Name
    52000-013Ice Cold Analgesic GelMenthol and Camphor
    52000-004Allure Ice Cold AnalgesicMenthol and Camphor
    66525-056BEE BRAND MEDICATEDMENTHOL AND CAMPHOR
    69274-004Blue Ice Topical AnalgesicMenthol and Camphor
    69312-006Blue Ice Topical AnalgesicMenthol and Camphor
    69257-213CBD UNLIMITED MISTX TOPICAL ANALGESICmenthol and camphor
    73045-002CBD UNLIMITED MISTX TOPICAL ANALGESICMenthol and Camphor
    73045-004CBD UNLIMITED TOPICAL ANALGESICMenthol and Camphor
    61577-1010DR. WOLFES WARM THERAPYMENTHOL AND CAMPHOR
    52862-017Health Smart Blue Ice Topical AnalgesicMenthol and Camphor
    52920-134Ice Cold AnalgesicMenthol and Camphor
    55614-600Lung Choy Shung Pain Relief LiquidMenthol and Camphor
    50488-0410Menthol 10 percent plus Camphor 4 percentMenthol and Camphor
    70537-001Red OilMenthol and Camphor
    73423-011Relieve Well Pain ReliefMenthol and Camphor
    69257-211Sigform Herbal Musclementhol and camphor
    69257-212Sigform Herbal Musclementhol and camphor
    69257-210Sigform Herbal Muscle Mistmenthol and camphor
    61577-3234SORE NO MORE WARM THERAPYMENTHOL and CAMPHOR
    61577-4040SORE NO MORE WARM THERAPYMENTHOL and CAMPHOR
    55614-700WU YANG BRAND PAIN RELIEVING MEDICATEDMENTHOL AND CAMPHOR
    55614-740YULAM DIE DA WAN HUA PAIN RELIEVINGMenthol and Camphor

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