Label: MIDNIGHT CINEMA LA BELLE IN ROUGE 01. DANCING IN MONACO- dimethicone lipstick
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Contains inactivated NDC Code(s)
NDC Code(s): 70905-0016-1 - Packager: Dr. Althea
- 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 April 14, 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
- PURPOSE
- KEEP OUT OF REACH OF CHILDREN
- INDICATIONS & USAGE
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WARNINGS
Caution：
1. If the following symptoms occur after using the product , stop using the product immediately and consult with a dermatologist
(1) Occurrence of red spots, swelling, itchiness, and other skin stimulation.
(2) If the symptoms above occur after the application area being exposed to direct sunlight
2. Do not use on wounds.
3. Precaution for Storage and Handling
(1) Keep out of reach of infants and children
(2) Do not store in a place exposed to direct sunlight.
- DOSAGE & ADMINISTRATION
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
MIDNIGHT CINEMA LA BELLE IN ROUGE 01. DANCING IN MONACO
dimethicone lipstickProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:70905-0016 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength DIMETHICONE (UNII: 92RU3N3Y1O) (DIMETHICONE - UNII:92RU3N3Y1O) DIMETHICONE 7.4 g in 100 g Inactive Ingredients Ingredient Name Strength TITANIUM DIOXIDE (UNII: 15FIX9V2JP) .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:70905-0016-1 1 g in 1 APPLICATOR; Type 0: Not a Combination Product 04/01/2017 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 04/01/2017 Labeler - Dr. Althea (689694436) Registrant - Dr. Althea (689694436) Establishment Name Address ID/FEI Business Operations Dr. Althea 689694436 manufacture(70905-0016) , label(70905-0016) , pack(70905-0016)
