NDC 51414-101

aloe vera gel

Aloe Vera Leaf

aloe vera 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 Aloe Vera Leaf.

Product ID51414-101_6207ccff-c165-d345-e053-2991aa0a803b
NDC51414-101
Product TypeHuman Otc Drug
Proprietary Namealoe vera gel
Generic NameAloe Vera Leaf
Dosage FormGel
Route of AdministrationTOPICAL
Marketing Start Date2014-05-08
Marketing CategoryOTC MONOGRAPH NOT FINAL / OTC MONOGRAPH NOT FINAL
Application Numberpart356
Labeler NameYuyao Jessie Commodity Co.,Ltd.
Substance NameALOE VERA LEAF
Active Ingredient Strength5 g/100g
NDC Exclude FlagN
Listing Certified Through2020-12-31

Packaging

NDC 51414-101-01

15 g in 1 PACKAGE (51414-101-01)
Marketing Start Date2018-01-05
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 51414-101-07 [51414010107]

aloe vera gel GEL
Marketing CategoryOTC monograph not final
Application Numberpart356
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-05

NDC 51414-101-01 [51414010101]

aloe vera gel GEL
Marketing CategoryOTC monograph not final
Application Numberpart356
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-05

NDC 51414-101-06 [51414010106]

aloe vera gel GEL
Marketing CategoryOTC monograph not final
Application Numberpart356
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-05

NDC 51414-101-09 [51414010109]

aloe vera gel GEL
Marketing CategoryOTC monograph not final
Application Numberpart356
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-05

NDC 51414-101-05 [51414010105]

aloe vera gel GEL
Marketing CategoryOTC monograph not final
Application Numberpart356
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-05

NDC 51414-101-04 [51414010104]

aloe vera gel GEL
Marketing CategoryOTC monograph not final
Application Numberpart356
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-05

NDC 51414-101-08 [51414010108]

aloe vera gel GEL
Marketing CategoryOTC monograph not final
Application Numberpart356
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-05

NDC 51414-101-02 [51414010102]

aloe vera gel GEL
Marketing CategoryOTC monograph not final
Application Numberpart356
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-05

NDC 51414-101-03 [51414010103]

aloe vera gel GEL
Marketing CategoryOTC monograph not final
Application Numberpart356
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-05

Drug Details

Active Ingredients

IngredientStrength
ALOE VERA LEAF5 g/100g

OpenFDA Data

SPL SET ID:43a31aec-6db0-4715-bcaf-b345bf713c38
Manufacturer
UNII

NDC Crossover Matching brand name "aloe vera gel" or generic name "Aloe Vera Leaf"

NDCBrand NameGeneric Name
11344-747Aloe Vera GelLidocaine HCl, Menthol
30142-747Aloe Vera GelLidocaine HCl, Menthol
41250-093Aloe Vera GelLidocaine HCl
41250-747Aloe Vera GelLidocaine HCl, Menthol
47993-220Aloe Vera GelAloe Vera Gel
51414-101aloe vera gelALOE VERA LEAF
56062-747Aloe Vera GelLidocaine HCl, Menthol
63941-005Aloe Vera GelLidocaine HCl
72288-747Aloe Vera GelLidocaine HCl, Menthol
72476-747Aloe Vera GelLidocaine HCl, Menthol
68428-129Aloe Socotrina Kit RefillALOE VERA LEAF
71596-052BRING GREEN FRESH MASK ALOEALOE VERA LEAF
55882-6098HelloAloe vera leaf
70869-010Secret No 1ALOE VERA LEAF

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