ACNE C-PATCH- vitamin e patch

Acne C-Patch by

Drug Labeling and Warnings

Acne C-Patch by is a Otc medication manufactured, distributed, or labeled by NeoBiotech Global Corporation. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

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

INGREDIENTS AND APPEARANCE

ACNE C-PATCH 
vitamin e patch

Product 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)