NDC 24909-180

Terrasil SKIN REPAIR

Calendula, Thuja Occidentalis

Terrasil SKIN REPAIR is a Topical Ointment in the Human Otc Drug category. It is labeled and distributed by Aidance Skincare & Topical Solutions, Llc. The primary component is Calendula Officinalis Flower; Thuja Occidentalis Whole.

Product ID24909-180_557569db-26cc-4d1d-8fa3-c047ac2a0310
NDC24909-180
Product TypeHuman Otc Drug
Proprietary NameTerrasil SKIN REPAIR
Generic NameCalendula, Thuja Occidentalis
Dosage FormOintment
Route of AdministrationTOPICAL
Marketing Start Date2017-01-01
Marketing CategoryUNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC
Labeler NameAidance Skincare & Topical Solutions, LLC
Substance NameCALENDULA OFFICINALIS FLOWER; THUJA OCCIDENTALIS WHOLE
Active Ingredient Strength1 [hp_X]/g; [hp_X]/g
NDC Exclude FlagN
Listing Certified Through2020-12-31

Packaging

NDC 24909-180-14

14 g in 1 TUBE (24909-180-14)
Marketing Start Date2017-01-01
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 24909-180-50 [24909018050]

Terrasil SKIN REPAIR OINTMENT
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2017-01-01

NDC 24909-180-14 [24909018014]

Terrasil SKIN REPAIR OINTMENT
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2017-01-01

Drug Details

Active Ingredients

IngredientStrength
CALENDULA OFFICINALIS FLOWER1 [hp_X]/g

OpenFDA Data

SPL SET ID:433a49ee-8f79-43e3-8502-76862e68a2e6
Manufacturer
UNII

NDC Crossover Matching brand name "Terrasil SKIN REPAIR" or generic name "Calendula, Thuja Occidentalis"

NDCBrand NameGeneric Name
24909-131Terrasil Skin RepairAllantoin, Benzethonium Chloride
24909-132Terrasil Skin RepairAllantoin, Benzethonium Chloride
24909-180Terrasil SKIN REPAIRCalendula, Thuja Occidentalis
24909-181Terrasil SKIN REPAIRCalendula, Symphytum Officinale, Thuja Occidentalis
24909-168terrasil INFECTION PROTECTION WOUND CARECalendula, Thuja Occidentalis

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