Label: ALL DAY ERR DAY- niacinamide, zinc oxide liquid
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Contains inactivated NDC Code(s)
NDC Code(s): 74921-0002-1 - Packager: COSMEDIQUE 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 October 23, 2021
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
Aloe Barbadensis Leaf Water
Propanediol
Niacinamide
Glycerin
Zinc Oxide
Cucumis Sativus (Cucumber) Fruit Water
Bambusa Vulgaris Extract
Panthenol
Centella Asiatica Extract
Anthemis Nobilis Flower Extract
Cetearyl Alcohol
1,2-Hexanediol
Cetearyl Olivate
Sorbitan Olivate
Tocopheryl Acetate
Adenosine
Euterpe Oleracea Fruit Extract
Sodium Hyaluronate
Citric Acid
Madecassoside
Madecassic Acid
Asiaticoside
Calophyllum Tacamahaca Seed Extract
Houttuynia Cordata Extract
Olea Europaea (Olive) Leaf Extract
Ocimum Basilicum (Basil) Leaf Extract
Opuntia Ficus-Indica Extract
Nelumbium Speciosum Flower Extract
Hamamelis Virginiana (Witch Hazel) Leaf ExtractHyaluronic Acid
Hydroxydecyl Ubiquinone
Anemarrhena Asphodeloides Root Extract
Collagen Extractrh-Oligopeptide-1
- PURPOSE
- KEEP OUT OF REACH OF CHILDREN
- INDICATIONS & USAGE
-
WARNINGS
For external use only.
Flammable, keep away from fire or flame.
When using this product keep out of eyes. If contact with eyes occurs, rinse promptly and thoroughly with water.
Stop use and ask a doctor if significant irritation or sensitization develops.
Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.
- DOSAGE & ADMINISTRATION
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
ALL DAY ERR DAY
niacinamide, zinc oxide liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:74921-0002 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC OXIDE - UNII:SOI2LOH54Z) ZINC OXIDE 5 g in 100 mL NIACINAMIDE (UNII: 25X51I8RD4) (NIACINAMIDE - UNII:25X51I8RD4) NIACINAMIDE 5 g in 100 mL Inactive Ingredients Ingredient Name Strength PANTHENOL (UNII: WV9CM0O67Z) GLYCERIN (UNII: PDC6A3C0OX) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:74921-0002-1 50 mL in 1 BOTTLE; Type 0: Not a Combination Product 10/23/2021 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 04/01/2020 Labeler - COSMEDIQUE CO.,LTD. (687550306) Registrant - COSMEDIQUE CO.,LTD. (687550306) Establishment Name Address ID/FEI Business Operations COSMEDIQUE CO.,LTD. 687550306 manufacture(74921-0002)
