ACNE C-PATCH- vitamin e patch 
NeoBiotech Global Corporation

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.

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Acne C-Patch

Active ingredients

Vitamin E (3%)

Purpose

acne treatment

USes

temporarily relieves symptoms of

- Acne

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

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

Charcoal, Gelatin, Aluminum glycinate, Ethylennediaminetetraacetic acid, Disodium slat, Castor oil, Polyvinyl alcohol Partially neutralized polyacrylate, Pured water, Salt, Sorbitol, Tartarid acid

Keep out of reach of children

Keep out of reach of children. If swallowed, contact a Poison Control Center or get medical help immediately

Acne C-Patch

acne c-patch

ACNE C-PATCH 
vitamin e patch
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:70236-103
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
.ALPHA.-TOCOPHEROL (UNII: H4N855PNZ1) (.ALPHA.-TOCOPHEROL - UNII:H4N855PNZ1) .ALPHA.-TOCOPHEROL0.06 g  in 2 g
Inactive Ingredients
Ingredient NameStrength
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 CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:70236-103-027 in 1 POUCH02/10/2018
1NDC:70236-103-012 g in 1 PATCH; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
unapproved drug other02/10/2018
Labeler - NeoBiotech Global Corporation (080020820)
Registrant - NeoBiotech Global Corporation (080020820)
Establishment
NameAddressID/FEIBusiness Operations
NeoBiotech Global Corporation080020820manufacture(70236-103)

Revised: 2/2018
Document Id: 64dc75e2-e2a6-c4c4-e053-2991aa0a0cde
Set id: 64dc75e2-e2a5-c4c4-e053-2991aa0a0cde
Version: 2
Effective Time: 20180210
 
NeoBiotech Global Corporation