Acne C-Patch: Package Insert and Label Information

ACNE C-PATCH- .alpha.-tocopherol 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.

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
(click image for full-size original)

ACNE C-PATCH
vitamin e patch
Product Information
Product Type HUMAN OTC DRUG Item Code (Source) NDC:70236-103
Route of Administration TOPICAL DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
.ALPHA.-TOCOPHEROL (.ALPHA.-TOCOPHEROL) .ALPHA.-TOCOPHEROL 0.06 g in 2 g
Inactive Ingredients
Ingredient Name Strength
DIHYDROXYALUMINUM AMINOACETATE ANHYDROUS
EDETIC ACID
CASTOR OIL
ACTIVATED CHARCOAL
GELATIN, UNSPECIFIED
TARTARIC ACID
GLYCERIN
POLYVINYL ALCOHOL, UNSPECIFIED
WATER
SODIUM CHLORIDE
SORBITOL
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:70236-103-02 7 PATCH in 1 POUCH contains a PATCH (70236-103-01)
1 NDC:70236-103-01 2 g in 1 PATCH This package is contained within the POUCH (70236-103-02)
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 Operations
NeoBiotech Global Corporation 080020820 manufacture (70236-103)

Revised: 02/2018 NeoBiotech Global Corporation

DrugInserts.com provides trustworthy package insert and label information about marketed drugs as submitted by manufacturers to the US Food and Drug Administration. Package information is not reviewed or updated separately by DrugInserts.com. Every individual package label entry contains a unique identifier which can be used to secure further details directly from the US National Institutes of Health and/or the FDA.

As the leading independent provider of trustworthy medication information, we source our database directly from the FDA's central repository of drug labels and package inserts under the Structured Product Labeling standard. Our material is not intended as a substitute for direct consultation with a qualified health professional.

Terms of Use | Copyright © 2021. All Rights Reserved.