Label: PURIFYING CENTELLA SOOTHING MASK- limonene, linalool liquid
- NDC Code(s): 71217-0053-1, 71217-0053-2
- Packager: inthismorning co ltd
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: unapproved drug other
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.
Drug Label Information
Updated January 30, 2023
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- ACTIVE INGREDIENT
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INACTIVE INGREDIENT
Water+A11:A42
Dipropylene Glycol
Butylene Glycol
Glycerin
Hydroxyacetophenone
Carbomer
Allantoin
Betaine
Caffeine
Tromethamine
Polyglyceryl-10 Laurate
Polyglyceryl-10 Myristate
Caprylyl Glycol
Ethylhexylglycerin
1,2-Hexanediol
Disodium EDTA
Sodium Hyaluronate
Althaea Rosea Flower Extract
Hamamelis Virginiana (Witch Hazel) Water
Citrus Aurantium Bergamia (Bergamot) Fruit Oil
Centella Asiatica Extract
Pyrus Malus (Apple) Fruit Extract
Rosmarinus Officinalis (Rosemary) Leaf Oil
Maltodextrin
Moringa Oleifera Seed Extract
Caprylic/Capric Triglyceride
Pistacia Lentiscus (Mastic) Gum
Hydrogenated Lecithin
Spiraea Ulmaria Extract
Phenethyl Alcohol - PURPOSE
- KEEP OUT OF REACH OF CHILDREN
- INDICATIONS & USAGE
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WARNINGS
This product is for exeternal use only. Do not use for internal use
Storage and handling precautions
If possible, avoid direct sunlight and store in cool and area of low humidity in order to maintain the quality of the product and avoid misuse
Avoid placing the product near fire and store out in reach of children- consult a physician in case of abnormal symptoms, such as red spots, swelling or itching, or side effects in the areas of application due to direct light during or after using the product
- do not use on wounded area
- DOSAGE & ADMINISTRATION
- PRINCIPAL DISPLAY PANEL
-
INGREDIENTS AND APPEARANCE
PURIFYING CENTELLA SOOTHING MASK
limonene, linalool liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:71217-0053 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength LIMONENE, (+)- (UNII: GFD7C86Q1W) (LIMONENE, (+)- - UNII:GFD7C86Q1W) LIMONENE, (+)- 0.00371146 g in 100 g LINALOOL, (+/-)- (UNII: D81QY6I88E) (LINALOOL, (+/-)- - UNII:D81QY6I88E) LINALOOL, (+/-)- 0.00109203 g in 100 g Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) GLYCERIN (UNII: PDC6A3C0OX) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:71217-0053-2 6 in 1 PACKAGE 01/15/2023 1 NDC:71217-0053-1 25 g in 1 POUCH; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 01/15/2023 Labeler - inthismorning co ltd (695126076) Registrant - inthismorning co ltd (695126076) Establishment Name Address ID/FEI Business Operations cosmax inc 689049693 manufacture(71217-0053) Establishment Name Address ID/FEI Business Operations inthismorning co ltd 695126076 label(71217-0053)
