Label: DERMVEDA JOCK ITCH- olive extract, sulfur spray
- NDC Code(s): 83819-003-04
- Packager: Celcius Corp.
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: unapproved homeopathic
DISCLAIMER: This homeopathic product has not been evaluated by the Food and Drug Administration for safety or efficacy. FDA is not aware of scientific evidence to support homeopathy as effective.
Drug Label Information
Updated December 23, 2023
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- Drug Facts
- Active ingredient
- Purpose
- Uses
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Warnings
For external use only.
Do not use • on children under 2 years of age unless directed by a doctor.
• Avoid contact with eyes.When using this product • mild increase in irritation or burning may occur.
Stop use and ask a doctor if
• If symptoms persist or inflammation increases after 2 weeks of use or if the itch increases.
• Increase in redness on skin.Pregnant or Breast Feeding
• Ask a Health Professional before use. -
Directions
Do Not use on Children less than 2 Years
• Shake well before use. Spray directly on the affected area a few times thoroughly till the entire area is covered. Wait for about a minute till the solution gets absorbed for best results. Use atleast 2-3 times a day for atleast 3 Weeks till symptoms subside and Jock Itch is cleared.
- Other information
- Inactive ingredients
- Questions?
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SPL UNCLASSIFIED SECTION
NATURAL SKIN CARE
MADE WITH NATURAL INGREDIENTS
WITH MICRONIZED SULFUR
• NO-STING • NON-TOXIC
• SOOTHING. • DEODORIZER
• NATURAL • NON-STAINING
• FAST AND EFFECTIVEHOMEOPATHIC MEDICINE
Complete Natural Jock Itch Relief solution
No Synthetics
No Alcohol
No Parabens
No Chloridesmade with Love
Distributed by
Celcius Corp
21415 Civic Center Dr, Suite 100
Southfield, MI 48076
www.celsiusherbs.com - Packaging
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INGREDIENTS AND APPEARANCE
DERMVEDA JOCK ITCH
olive extract, sulfur sprayProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:83819-003 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength OLEA EUROPAEA LEAF (UNII: MJ95C3OH47) (OLEA EUROPAEA LEAF - UNII:MJ95C3OH47) OLEA EUROPAEA LEAF 8 [hp_X] in 118 mL SULFUR (UNII: 70FD1KFU70) (SULFUR - UNII:70FD1KFU70) SULFUR 6 [hp_X] in 118 mL Inactive Ingredients Ingredient Name Strength AZADIRACHTA INDICA SEED OIL (UNII: 4DKJ9B3K2T) GLYCERIN (UNII: PDC6A3C0OX) PEPPERMINT OIL (UNII: AV092KU4JH) OLIVE OIL (UNII: 6UYK2W1W1E) KARUM SEED OIL (UNII: 62160PU6FJ) CALAMUS OIL (UNII: 5F9K5X640P) TURMERIC (UNII: 856YO1Z64F) XANTHAN GUM (UNII: TTV12P4NEE) WATER (UNII: 059QF0KO0R) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:83819-003-04 118 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product 12/22/2023 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved homeopathic 12/22/2023 Labeler - Celcius Corp. (117755609)
