NDC 51393-4012

Wrinkle Control

Thuja Occidentalis Leaf

Wrinkle Control is a Topical Solution/ Drops in the Human Otc Drug category. It is labeled and distributed by Forces Of Nature. The primary component is Thuja Occidentalis Leaf.

Product ID51393-4012_089852c9-4482-45d0-a85d-d4fa7d0a79fe
NDC51393-4012
Product TypeHuman Otc Drug
Proprietary NameWrinkle Control
Generic NameThuja Occidentalis Leaf
Dosage FormSolution/ Drops
Route of AdministrationTOPICAL
Marketing Start Date2013-03-15
Marketing CategoryUNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC
Labeler NameForces of Nature
Substance NameTHUJA OCCIDENTALIS LEAF
Active Ingredient Strength6 [hp_X]/100mL
NDC Exclude FlagN
Listing Certified Through2019-12-31

Packaging

NDC 51393-4012-2

33 mL in 1 BOTTLE, DISPENSING (51393-4012-2)
Marketing Start Date2013-03-15
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 51393-4012-2 [51393401202]

Wrinkle Control SOLUTION/ DROPS
Marketing CategoryUNAPPROVED HOMEOPATHIC
Product TypeHUMAN OTC DRUG
Marketing Start Date2013-03-15
Inactivation Date2020-01-31

NDC 51393-4012-1 [51393401201]

Wrinkle Control SOLUTION/ DROPS
Marketing CategoryUNAPPROVED HOMEOPATHIC
Product TypeHUMAN OTC DRUG
Marketing Start Date2013-03-15
Inactivation Date2020-01-31

Drug Details

Active Ingredients

IngredientStrength
THUJA OCCIDENTALIS LEAF6 [hp_X]/100mL

OpenFDA Data

SPL SET ID:afd92705-bd32-48f6-a322-7f44df41b973
Manufacturer
UNII

NDC Crossover Matching brand name "Wrinkle Control" or generic name "Thuja Occidentalis Leaf"

NDCBrand NameGeneric Name
51393-4012Wrinkle ControlTHUJA OCCIDENTALIS LEAF
51393-4007Scabies ControlTHUJA OCCIDENTALIS LEAF

Trademark Results [Wrinkle Control]

Mark Image

Registration | Serial
Company
Trademark
Application Date
WRINKLE CONTROL
WRINKLE CONTROL
77775212 3795260 Dead/Cancelled
pac fung feather co., ltd.
2009-07-07
WRINKLE CONTROL
WRINKLE CONTROL
77412504 not registered Dead/Abandoned
Heuer, Marvin A.
2008-03-04

© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.