DRS. PHARMACY SCAR CREAM- allantoin cream

Drs. pharmacy Scar Cream by

Drug Labeling and Warnings

Drs. pharmacy Scar Cream by is a Otc medication manufactured, distributed, or labeled by OL PHARMA TECH, LLC Drs PHARMACY. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Allantoin 0.5%

DOSAGE & ADMINISTRATION

Dosage and Administration: Gently massage into scar twice a day for 2-3 minutes

PURPOSE

Purpose: Skin Protectant

INDICATIONS & USAGE

Indication and Usage: Temporarily protects and helps relieve chapped or cracked skin.

Inactive Ingredients

Cetostearyl alcohol- mineral oil- ceteareth 20- propylene glycol- methyl paraben- propylparaben- vitamin E- Stearic acid - trolamine RosmarinusOfficinalis (Rosemary)Extract/ Portulaca Oleracea Extract/Thymus Vulgaris Thyme) Leaf Extract/Jasminum Officinale (jasmine) Flower/ Leaf Extract?Chamomila) Recutita (Matricaria) Flower Water, Aureobasidium Pullulans Ferment Extract/ 1.2-Hexanedio

Warnings

• In case of having the following symptoms after using this cream, you are advised to stop using it immediately. If you keep using it , the symptoms will get worse and need to consult a drematologist .1- in case of having problems such as red rash, swollllenness, itching, stimulation during usage. 2- in case of having the same symptoms above on the part you put this product on by direct sunlight
• you are banned to use it on the part where you have a eczema, lor dermatitis.
• in case of getting it into your eyes, you have to wash it immediately.

Questions

drspharmacy.com

KEEP OUT OF REACH OF CHILDREN

Keep out of reach of children and babies

package label

INGREDIENTS AND APPEARANCE

DRS. PHARMACY SCAR CREAM 
allantoin cream

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 80489-333
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALLANTOIN (UNII: 344S277G0Z) (ALLANTOIN - UNII:344S277G0Z)	ALLANTOIN	0.5 g  in 100 g

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
TROLAMINE (UNII: 9O3K93S3TK)
.ALPHA.-TOCOPHEROL (UNII: H4N855PNZ1)
EDETATE DISODIUM (UNII: 7FLD91C86K)
CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
STEARIC ACID (UNII: 4ELV7Z65AP)
MINERAL OIL (UNII: T5L8T28FGP)
METHYLPARABEN (UNII: A2I8C7HI9T)
THYMUS VULGARIS LEAF (UNII: GRX3499643)
1,2-HEXANEDIOL (UNII: TR046Y3K1G)
JASMINUM OFFICINALE FLOWER (UNII: 0Q8K841432)
MATRICARIA CHAMOMILLA LEAF (UNII: 6I9LN466F0)
ROSMARINUS OFFICINALIS WHOLE (UNII: EA3289138M)
PORTULACA OLERACEA WHOLE (UNII: D5J3623SV2)
POLYOXYL 20 CETOSTEARYL ETHER (UNII: YRC528SWUY)
PROPYLPARABEN (UNII: Z8IX2SC1OH)

Product Characteristics
Color	white	Score
Shape		Size
Flavor		Imprint Code
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 80489-333-01	1 in 1 CARTON	11/01/2021
1		20 g in 1 TUBE; Type 0: Not a Combination Product
2	NDC: 80489-333-02	1 in 1 CARTON	11/01/2021
2		30 g in 1 TUBE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M016	11/01/2021

Labeler - OL PHARMA TECH, LLC Drs PHARMACY (021170377)

Establishment
Name	Address	ID/FEI	Business Operations
OL PHARMA TECH, LLC Drs PHARMACY		021170377	manufacture(80489-333)