ADVANCED RELIEF A AND D- petrolatum ointment

Ülke: ABD

Dil: İngilizce

Kaynak: NLM (National Library of Medicine)

Aktif bileşen:

PETROLATUM (UNII: 4T6H12BN9U) (PETROLATUM - UNII:4T6H12BN9U)

Mevcut itibaren:

Ultra Seal Corporation

INN (International Adı):

PETROLATUM

Kompozisyon:

PETROLATUM 937.5 mg in 1 g

Uygulama yolu:

TOPICAL

Reçete türü:

OTC DRUG

Terapötik endikasyonlar:

Purpose-Skin Protectant Uses-Temporarily protects minor cuts, scrapes, and burns.  Temporarily protects and helps chapped or cracked skin and lips.  Helps protect lips from drying effects of wind and cold weather.

Yetkilendirme durumu:

OTC monograph final

Ürün özellikleri

ADVANCED RELIEF A AND D- PETROLATUM OINTMENT
ULTRA SEAL CORPORATION
_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._
----------
Active Ingredient (in each gram): White Petrolatum 93.5%
Purpose-Skin Protectant
Uses-Temporarily protects minor cuts, scrapes, and burns. Temporarily
protects and helps chapped or
cracked skin and lips. Helps protect lips from drying effects of wind
and cold weather.
Directions: Apply as needed
Keep out of reach of children. If swallowed, get medical help or
contact a Poison Control Center right
away.
For external use only. Do not use in eyes, on deep puncture wounds,
animal bites, or serious burns or
for more than 1 week unless directed by a doctor.
Stop use and ask a doctor if: A rash or allergic reaction develops.
Condition worsens, persists, or
recurs.
Inactive Ingredients: Corn Oil, Light Mineral Oil, Vitamin A
Palmitate, Vitamin D
ADVANCED RELIEF A AND D
petrolatum ointment
PRODUCT INFORMATION
PRODUCT T YPE
HUMAN OTC DRUG
ITE M CODE (SOURCE )
NDC:42213-375
ROUTE OF ADMINISTRATION
TOPICAL
ACTIVE INGREDIENT/ACTIVE MOIETY
INGREDIENT NAME
BASIS OF STRENGTH
STRE NG TH
PETRO LATUM (UNII: 4T6 H12BN9 U) (PETROLATUM - UNII:4T6 H12BN9 U)
PETROLATUM
9 37.5 mg in 1 g
INACTIVE INGREDIENTS
Ultra Seal Corporation
INGREDIENT NAME
STRE NG TH
MINERAL O IL (UNII: T5L8 T28 FGP)
CO RN O IL (UNII: 8 470 G57WFM)
VITAMIN A PALMITATE (UNII: 1D1K0 N0 VVC)
ERGO CALCIFERO L (UNII: VS0 41H42XC)
PACKAG ING
#
ITEM CODE
PACKAGE DESCRIPTION
MARKETING START DATE
MARKETING END DATE
1
NDC:42213-375-47
144 in 1 CARTON
12/0 1/20 11
1
NDC:42213-375-0 5
5 g in 1 PACKET; Type 0 : No t a Co mbinatio n Pro duct
MARKETING INFORMATION
MARKE TING CATE GORY
APPLICATION NUMBE R OR MONOGRAPH CITATION
MARKE TING START DATE
MARKE TING END DATE
OTC mo no graph final
pa rt347
12/0 1/20 11
LABELER -
Ultra Seal Corporation (085752004)
REGISTRANT -
ULT RAtab Laboratories, Inc. (1