Label: SONATURAL ALL KILL BLACKHEAD CLEAR- silica stick
-
Contains inactivated NDC Code(s)
NDC Code(s): 71322-160-01, 71322-160-02 - Packager: Sonatural Global 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 November 29, 2017
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- ACTIVE INGREDIENT
-
INACTIVE INGREDIENT
Inactive ingredients: Water, Propylene Glycol, Sodium Stearate, Butylene Glycol, Bis-PEG-15 Methyl Ether Dimethicone, Polysorbate 20,1,2-Hexanediol, Bentonite, Lactose, Cellulose, Hydroxypropyl Methylcellulose, Jojoba Esters, Tocopheryl Acetate, Ascorbyl Palmitate, Retinyl Palmitate, Charcoal Powder, Vitis Vinifera (Grape) Seed Oil, Prunus Armeniaca (Apricot) Kernel Oil, Calendula Officinalis Flower Oil, Squalane, Sodium Hyaluronate, Ethylhexylglycerin, Glyceryl Caprylate, CI 77492, CI 77499
- PURPOSE
-
WARNINGS
Warnings: 1. If the following symptoms occur, discontinue use and consult a dermatologist: 1) Red spots, swelling, itchiness, or irritation upon use 2) If above symptoms occur when skin is in direct sunlight 2. Do not use on open wounds and on skin with eczema or dermatitis 3. Storage instructions: 1) Keep out of reach of children 2) Store at room temperature away from direct sunlight 4. Avoid contact with eyes 5. Be aware of the grain and avoid contact with eyes 6. Rinse with water immediately if the grain contact with eyes and stop use and ask a doctor if any symptoms occur
- KEEP OUT OF REACH OF CHILDREN
- Uses
- Directions
- QUESTIONS
- PACKAGE LABEL.PRINCIPAL DISPLAY PANEL
-
INGREDIENTS AND APPEARANCE
SONATURAL ALL KILL BLACKHEAD CLEAR
silica stickProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:71322-160 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength SILICON DIOXIDE (UNII: ETJ7Z6XBU4) (SILICON DIOXIDE - UNII:ETJ7Z6XBU4) SILICON DIOXIDE 0.88 g in 11 g Inactive Ingredients Ingredient Name Strength Water (UNII: 059QF0KO0R) Propylene Glycol (UNII: 6DC9Q167V3) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:71322-160-02 1 in 1 CARTON 10/01/2017 1 NDC:71322-160-01 11 g in 1 CONTAINER; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 10/01/2017 Labeler - Sonatural Global Co.,Ltd (694818511) Registrant - Sonatural Global Co.,Ltd (694818511) Establishment Name Address ID/FEI Business Operations Sonatural Global Co.,Ltd 694818511 manufacture(71322-160)
