NDC 58133-950

RelieveIt SprainGo Gel

Arnica Montana, Ruta Graveolens, Symphytum Officinale, Mentha Piperita (peppermint)

RelieveIt SprainGo Gel is a Topical Gel in the Human Otc Drug category. It is labeled and distributed by Cosmetic Specialty Labs, Inc.. The primary component is Arnica Montana; Mentha Piperita; Symphytum Officinale Whole; Ruta Graveolens Flowering Top Oil.

Product ID58133-950_7871bbc1-9f10-3f94-e053-2a91aa0a7b5a
NDC58133-950
Product TypeHuman Otc Drug
Proprietary NameRelieveIt SprainGo Gel
Generic NameArnica Montana, Ruta Graveolens, Symphytum Officinale, Mentha Piperita (peppermint)
Dosage FormGel
Route of AdministrationTOPICAL
Marketing Start Date2018-10-17
Marketing CategoryUNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC
Labeler NameCosmetic Specialty Labs, Inc.
Substance NameARNICA MONTANA; MENTHA PIPERITA; SYMPHYTUM OFFICINALE WHOLE; RUTA GRAVEOLENS FLOWERING TOP OIL
Active Ingredient Strength7 [hp_M]/mL; [hp_M]/mL; [hp_M]/mL; [hp_M]/mL
NDC Exclude FlagN
Listing Certified Through2020-12-31

Packaging

NDC 58133-950-02

70 mL in 1 BOTTLE, PUMP (58133-950-02)
Marketing Start Date2018-10-17
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 58133-950-16 [58133095016]

RelieveIt SprainGo Gel GEL
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-10-17

NDC 58133-950-37 [58133095037]

RelieveIt SprainGo Gel GEL
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-10-17

NDC 58133-950-02 [58133095002]

RelieveIt SprainGo Gel GEL
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-10-17

Drug Details

Active Ingredients

IngredientStrength
ARNICA MONTANA7 [hp_M]/mL

OpenFDA Data

SPL SET ID:7871bbc1-9f0f-3f94-e053-2a91aa0a7b5a
Manufacturer
UNII

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