Label: DIMETHICONE- cyclomethicone patch
- NDC Code(s): 83490-316-01
- Packager: 2359 US INC
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: unapproved drug other
DISCLAIMER: This drug has not been found by FDA to be safe and effective, and this labeling has not been approved by FDA. For further information about unapproved drugs, click here.
Drug Label Information
Updated June 1, 2023
If you are a consumer or patient please visit this version.
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- Active Ingredients
- Purposes
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Uses
Oia is here to fix all wrinkle worries! Oia silicone patches gently compress and protect the skin to noticeably minimize the appearance of fine lines and wrinkles. Our patches are the fastest anf safest way to achieve anti-aging effects. You can leave them on while you relax or even while you sleep!
- Warnings
- Warnings
- Warnings
- Warnings
- Warnings
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Directions
STEP 1- Thoroughly cleanse and dry your skin before usage. Allow skincare to properly absorb prior to patch applisction as excess misture might cause the patches to slide off.
STEP 2- Carefully remove the seal from the patch and position above the desired area. Make sure to streych the surface of your skin as much as possible before application.
STEP 3- After you apply the patch, gently press onto it ti flatten out any air bubbles that may form.
STEP 4- After use, rinse the patches with just water(or with mild soap) and allow the patches to air dry adhesive side up before storing back on the sheet provided.
- Inactive Ingredients
- Label
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INGREDIENTS AND APPEARANCE
DIMETHICONE
cyclomethicone patchProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:83490-316 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength DIMETHICONE (UNII: 92RU3N3Y1O) (DIMETHICONE - UNII:92RU3N3Y1O) DIMETHICONE 48 g in 100 g Inactive Ingredients Ingredient Name Strength CYCLOMETHICONE (UNII: NMQ347994Z) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:83490-316-01 48 g in 1 POUCH; Type 0: Not a Combination Product 06/01/2023 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 06/01/2023 Labeler - 2359 US INC (118974080) Registrant - 2359 US INC (118974080) Establishment Name Address ID/FEI Business Operations isamogu Inc. 695695834 manufacture(83490-316)