Label: ACNE C-PATCH- vitamin e patch
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Contains inactivated NDC Code(s)
NDC Code(s): 70236-103-01, 70236-103-02 - Packager: NeoBiotech Global Corporation
- 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 February 10, 2018
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- Active ingredients
- Purpose
- USes
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Warnings
For external use only
When using this product
Use only as directed.
- Do not bandage tightly or use with heating pad
- Avoid contact with eyes and mucus membranes
- Do not appy wounds or broken skin
- Do not apply to large areas of the body
- In case of deep or puncture wounds, animal bites or serious burns, consult a doctor
Stop use and ask a doctor if
- condition worsen
- irritation develops
- symptoms persist for more than 7 days or recurs within 1 day of discontinuation
- do not use for more than 7 days
If pregnant or breast-feeding, ask a health professional before use
Keep out of reach of children. If swallowd, contact a Poison Control Center or get medical help immediatel
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Directions
Adults and children over 12 years:
- Clean affected skin
- Remove film from patch
- Carefully apply the patch to the affected region and press skin firmly
- Patch can remain on the skin for up to 8 hours
- May repeat as necessary up to a maximum of 3 times per day
- For tick and bee stings, remove tick or stinger before applying patch
Children 12 years and younger: ask a health professional
- Inactive ingredients
- Keep out of reach of children
- Acne C-Patch
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INGREDIENTS AND APPEARANCE
ACNE C-PATCH
vitamin e patchProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:70236-103 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength .ALPHA.-TOCOPHEROL (UNII: H4N855PNZ1) (.ALPHA.-TOCOPHEROL - UNII:H4N855PNZ1) .ALPHA.-TOCOPHEROL 0.06 g in 2 g Inactive Ingredients Ingredient Name Strength DIHYDROXYALUMINUM AMINOACETATE ANHYDROUS (UNII: 1K713C615K) EDETIC ACID (UNII: 9G34HU7RV0) CASTOR OIL (UNII: D5340Y2I9G) ACTIVATED CHARCOAL (UNII: 2P3VWU3H10) GELATIN, UNSPECIFIED (UNII: 2G86QN327L) TARTARIC ACID (UNII: W4888I119H) GLYCERIN (UNII: PDC6A3C0OX) POLYVINYL ALCOHOL, UNSPECIFIED (UNII: 532B59J990) WATER (UNII: 059QF0KO0R) SODIUM CHLORIDE (UNII: 451W47IQ8X) SORBITOL (UNII: 506T60A25R) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:70236-103-02 7 in 1 POUCH 02/10/2018 1 NDC:70236-103-01 2 g in 1 PATCH; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 02/10/2018 Labeler - NeoBiotech Global Corporation (080020820) Registrant - NeoBiotech Global Corporation (080020820) Establishment Name Address ID/FEI Business Operations NeoBiotech Global Corporation 080020820 manufacture(70236-103)
