NDC 51414-909

Pain Relieving Burn Gel

Burn Gel

Pain Relieving Burn Gel is a Topical Gel in the Human Otc Drug category. It is labeled and distributed by Yuyao Jessie Commodity Co.,ltd.. The primary component is Lidocaine.

Product ID51414-909_7eafa811-75c3-077f-e053-2991aa0a8af0
NDC51414-909
Product TypeHuman Otc Drug
Proprietary NamePain Relieving Burn Gel
Generic NameBurn Gel
Dosage FormGel
Route of AdministrationTOPICAL
Marketing Start Date2019-01-01
Marketing CategoryOTC MONOGRAPH FINAL / OTC MONOGRAPH FINAL
Application Numberpart346
Labeler NameYuyao Jessie Commodity Co.,Ltd.
Substance NameLIDOCAINE
Active Ingredient Strength2 g/100g
NDC Exclude FlagN
Listing Certified Through2020-12-31

Packaging

NDC 51414-909-01

.5 g in 1 PACKAGE (51414-909-01)
Marketing Start Date2019-01-04
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 51414-909-08 [51414090908]

Pain Relieving Burn Gel GEL
Marketing CategoryOTC monograph final
Application Numberpart346
Product TypeHUMAN OTC DRUG
Marketing Start Date2019-01-04

NDC 51414-909-11 [51414090911]

Pain Relieving Burn Gel GEL
Marketing CategoryOTC monograph final
Application Numberpart346
Product TypeHUMAN OTC DRUG
Marketing Start Date2019-01-01

NDC 51414-909-15 [51414090915]

Pain Relieving Burn Gel GEL
Marketing CategoryOTC monograph final
Application Numberpart346
Product TypeHUMAN OTC DRUG
Marketing Start Date2019-01-01

NDC 51414-909-12 [51414090912]

Pain Relieving Burn Gel GEL
Marketing CategoryOTC monograph final
Application Numberpart346
Product TypeHUMAN OTC DRUG
Marketing Start Date2019-01-04

NDC 51414-909-20 [51414090920]

Pain Relieving Burn Gel GEL
Marketing CategoryOTC monograph final
Application Numberpart346
Product TypeHUMAN OTC DRUG
Marketing Start Date2019-01-04

NDC 51414-909-09 [51414090909]

Pain Relieving Burn Gel GEL
Marketing CategoryOTC monograph final
Application Numberpart346
Product TypeHUMAN OTC DRUG
Marketing Start Date2019-01-04

NDC 51414-909-17 [51414090917]

Pain Relieving Burn Gel GEL
Marketing CategoryOTC monograph final
Application Numberpart346
Product TypeHUMAN OTC DRUG
Marketing Start Date2019-01-04

NDC 51414-909-02 [51414090902]

Pain Relieving Burn Gel GEL
Marketing CategoryOTC monograph final
Application Numberpart346
Product TypeHUMAN OTC DRUG
Marketing Start Date2019-01-04

NDC 51414-909-22 [51414090922]

Pain Relieving Burn Gel GEL
Marketing CategoryOTC monograph final
Application Numberpart346
Product TypeHUMAN OTC DRUG
Marketing Start Date2019-01-04

NDC 51414-909-03 [51414090903]

Pain Relieving Burn Gel GEL
Marketing CategoryOTC monograph final
Application Numberpart346
Product TypeHUMAN OTC DRUG
Marketing Start Date2019-01-04

NDC 51414-909-21 [51414090921]

Pain Relieving Burn Gel GEL
Marketing CategoryOTC monograph final
Application Numberpart346
Product TypeHUMAN OTC DRUG
Marketing Start Date2019-01-04

NDC 51414-909-05 [51414090905]

Pain Relieving Burn Gel GEL
Marketing CategoryOTC monograph final
Application Numberpart346
Product TypeHUMAN OTC DRUG
Marketing Start Date2019-01-04

NDC 51414-909-16 [51414090916]

Pain Relieving Burn Gel GEL
Marketing CategoryOTC monograph final
Application Numberpart346
Product TypeHUMAN OTC DRUG
Marketing Start Date2019-01-04

NDC 51414-909-07 [51414090907]

Pain Relieving Burn Gel GEL
Marketing CategoryOTC monograph final
Application Numberpart346
Product TypeHUMAN OTC DRUG
Marketing Start Date2019-01-04

NDC 51414-909-01 [51414090901]

Pain Relieving Burn Gel GEL
Marketing CategoryOTC monograph final
Application Numberpart346
Product TypeHUMAN OTC DRUG
Marketing Start Date2019-01-04

NDC 51414-909-19 [51414090919]

Pain Relieving Burn Gel GEL
Marketing CategoryOTC monograph final
Application Numberpart346
Product TypeHUMAN OTC DRUG
Marketing Start Date2019-01-04

NDC 51414-909-10 [51414090910]

Pain Relieving Burn Gel GEL
Marketing CategoryOTC monograph final
Application Numberpart346
Product TypeHUMAN OTC DRUG
Marketing Start Date2019-01-04

NDC 51414-909-25 [51414090925]

Pain Relieving Burn Gel GEL
Marketing CategoryOTC monograph final
Application Numberpart346
Product TypeHUMAN OTC DRUG
Marketing Start Date2019-01-04

NDC 51414-909-04 [51414090904]

Pain Relieving Burn Gel GEL
Marketing CategoryOTC monograph final
Application Numberpart346
Product TypeHUMAN OTC DRUG
Marketing Start Date2019-01-04

NDC 51414-909-24 [51414090924]

Pain Relieving Burn Gel GEL
Marketing CategoryOTC monograph final
Application Numberpart346
Product TypeHUMAN OTC DRUG
Marketing Start Date2019-01-04

NDC 51414-909-18 [51414090918]

Pain Relieving Burn Gel GEL
Marketing CategoryOTC monograph final
Application Numberpart346
Product TypeHUMAN OTC DRUG
Marketing Start Date2019-01-04

NDC 51414-909-06 [51414090906]

Pain Relieving Burn Gel GEL
Marketing CategoryOTC monograph final
Application Numberpart346
Product TypeHUMAN OTC DRUG
Marketing Start Date2019-01-04

NDC 51414-909-13 [51414090913]

Pain Relieving Burn Gel GEL
Marketing CategoryOTC monograph final
Application Numberpart346
Product TypeHUMAN OTC DRUG
Marketing Start Date2019-01-04

NDC 51414-909-14 [51414090914]

Pain Relieving Burn Gel GEL
Marketing CategoryOTC monograph final
Application Numberpart346
Product TypeHUMAN OTC DRUG
Marketing Start Date2019-01-04

NDC 51414-909-23 [51414090923]

Pain Relieving Burn Gel GEL
Marketing CategoryOTC monograph final
Application Numberpart346
Product TypeHUMAN OTC DRUG
Marketing Start Date2019-01-04

Drug Details

Active Ingredients

IngredientStrength
LIDOCAINE2 g/100g

OpenFDA Data

SPL SET ID:7eafa811-75c1-077f-e053-2991aa0a8af0
Manufacturer
UNII
RxNorm Concept Unique ID - RxCUI
  • 2107764

    • NDC Crossover Matching brand name "Pain Relieving Burn Gel" or generic name "Burn Gel"

    NDCBrand NameGeneric Name
    51414-909Pain Relieving Burn GelBurn Gel
    71105-096Rediburn Burn Gel Skin ProtectantBurn Gel
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