DERMAMED- skin protectant ointment

Quốc gia: Hoa Kỳ

Ngôn ngữ: Tiếng Anh

Nguồn: NLM (National Library of Medicine)

Thành phần hoạt chất:

ALUMINUM HYDROXIDE (UNII: 5QB0T2IUN0) (ALUMINUM HYDROXIDE - UNII:5QB0T2IUN0)

Sẵn có từ:

DermaRite Industries, LLC

Tuyến hành chính:

TOPICAL

Loại thuốc theo toa:

OTC DRUG

Chỉ dẫn điều trị:

Skin protectant Dries the oozing and weeping of poison: ivy, oak, or sumac, or other skin irritations.

Tình trạng ủy quyền:

OTC monograph final

Đặc tính sản phẩm

DERMAMED- SKIN PROTECTANT OINTMENT
DERMARITE INDUSTRIES, LLC
_Disclaimer: Most OTC drugs are not reviewed and approved by FDA,
however they may be marketed if they_
_comply with applicable regulations and policies. FDA has not
evaluated whether this product complies._
----------
DERMAMED
ACTIVE INGREDIENT
Aluminum Hydroxide Gel 2%
PURPOS E
Skin protectant
US ES
Dries the oozing and weeping of poison: ivy, oak, or sumac, or other
skin irritations.
WARNINGS
FOR EXTERNAL USE ONLY.
AVOID CONTACT WITH EYES. In case of contact, flush thoroughly with
water.
WARNINGS
STOP AND ASK A DOCTOR IF
condition worsens
symptoms last more than 7 days or clear up and occur again within a
few days
WARNINGS
KEEP OUT OF REACH OF CHILDREN.
In case of accidental ingestion contact a Physician or Poison Control
Center right away.
DIRECTIONS
Apply liberally to the affected area as needed or as directed by a
physician.
OTHER INFORMATION
Store at room temperature (59º- 86ºF)
You may report a serious adverse event to DermaRite Industries, PO Box
7209, North Bergen, NJ
07047.
INACTIVE INGREDIENTS
Petrolatum, Lanolin, Water, Propylene Glycol, Stearyl Alcohol, Calcium
Carbonate, Magnesium
Hydroxide, Zinc Chloride, DMDM Hydantoin, Methylparaben,
Propylparaben, Sodium Laureth Sulfate,
Lanolin Alcohol, Cholecalciferol, Zea Mays (Corn) Oil, Retinyl
Palmitate, Citric Acid, Sodium
Chloride
QUES TIONS ?
Call 800-337-6296 Mon - Fri 9AM - 5PM EST.
DERMAMED PACKAGE LABEL AND PRINCIPAL DISPLAY PANEL
DERMAMED
skin protectant ointment
PRODUCT INFORMATION
PRODUCT T YPE
HUMAN OTC DRUG
ITE M CODE (SOURCE )
NDC:6 19 24-214
ROUTE OF ADMINISTRATION
TOPICAL
ACTIVE INGREDIENT/ACTIVE MOIETY
INGREDIENT NAME
BASIS OF STRENGTH
STRE NG TH
ALUMINUM HYDRO XIDE (UNII: 5QB0 T2IUN0 ) (ALUMINUM HYDROXIDE -
UNII:5QB0 T2IUN0 )
ALUMINUM
HYDROXIDE
2 g
in 10 0 g
INACTIVE INGREDIENTS
INGREDIENT NAME
STRE NG TH
CHO LECALCIFERO L (UNII: 1C6 V77QF41)
LANO LIN (UNII: 7EV6 5EAW6 H)
LANO LIN ALCO HO LS (UNII: 8 8 4C3FA9 HE)
SO DIUM LAURETH SULFATE (UNII: BPV39 0 UAP0 )
MAGNESIUM HYDRO XI