NDC 73016-003 Actibeau Camellia Natural Mineral Uv Defense Sunscreen

Zinc Oxide, Titanium Dioxide

NDC Product Code 73016-003

NDC Code: 73016-003

Proprietary Name: Actibeau Camellia Natural Mineral Uv Defense Sunscreen What is the Proprietary Name?
The proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.

Non-Proprietary Name: Zinc Oxide, Titanium Dioxide What is the Non-Proprietary Name?
The non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.

NDC Code Structure

  • 73016 - Activebeuty Co.,ltd
    • 73016-003 - Actibeau Camellia Natural Mineral Uv Defense Sunscreen

NDC 73016-003-02

Package Description: 1 CONTAINER in 1 CARTON > 50 mL in 1 CONTAINER (73016-003-01)

NDC Product Information

Actibeau Camellia Natural Mineral Uv Defense Sunscreen with NDC 73016-003 is a a human over the counter drug product labeled by Activebeuty Co.,ltd. The generic name of Actibeau Camellia Natural Mineral Uv Defense Sunscreen is zinc oxide, titanium dioxide. The product's dosage form is cream and is administered via topical form.

Labeler Name: Activebeuty Co.,ltd

Dosage Form: Cream - An emulsion, semisolid3 dosage form, usually containing > 20% water and volatiles5 and/or < 50% hydrocarbons, waxes, or polyols as the vehicle. This dosage form is generally for external application to the skin or mucous membranes.

Product Type: Human Otc Drug What kind of product is this?
Indicates the type of product, such as Human Prescription Drug or Human Over the Counter Drug. This data element matches the “Document Type” field of the Structured Product Listing.

Actibeau Camellia Natural Mineral Uv Defense Sunscreen Active Ingredient(s)

What is the Active Ingredient(s) List?
This is the active ingredient list. Each ingredient name is the preferred term of the UNII code submitted.

  • ZINC OXIDE 109.52 mg/mL
  • TITANIUM DIOXIDE 48.187 mg/mL

Inactive Ingredient(s)

About the Inactive Ingredient(s)
The inactive ingredients are all the component of a medicinal product OTHER than the active ingredient(s). The acronym "UNII" stands for “Unique Ingredient Identifier” and is used to identify each inactive ingredient present in a product.

  • WATER (UNII: 059QF0KO0R)
  • CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)
  • MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U)
  • BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
  • ETHYLHEXYL PALMITATE (UNII: 2865993309)
  • COCONUT OIL (UNII: Q9L0O73W7L)
  • CETYL PEG/PPG-10/1 DIMETHICONE (HLB 2) (UNII: V2W71V8T0X)
  • DICAPRYLYL CARBONATE (UNII: 609A3V1SUA)
  • NIACINAMIDE (UNII: 25X51I8RD4)
  • ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)
  • GLYCERIN (UNII: PDC6A3C0OX)
  • 1,2-HEXANEDIOL (UNII: TR046Y3K1G)
  • SODIUM CHLORIDE (UNII: 451W47IQ8X)
  • CAPRYLYL TRISILOXANE (UNII: Q95M2P1KJL)
  • QUATERNIUM-18 HECTORITE (UNII: IIS3YBV1XX)
  • CANDELILLA WAX (UNII: WL0328HX19)
  • DIMETHICONE CROSSPOLYMER (450000 MPA.S AT 12% IN CYCLOPENTASILOXANE) (UNII: UF7620L1W6)
  • ALUMINUM HYDROXIDE (UNII: 5QB0T2IUN0)
  • BORON NITRIDE (UNII: 2U4T60A6YD)
  • PENTAERYTHRITYL TETRAETHYLHEXANOATE (UNII: XJ7052W897)
  • SORBITAN ISOSTEARATE (UNII: 01S2G2C1E4)
  • POLYHYDROXYSTEARIC ACID (2300 MW) (UNII: YXH47AOU0F)
  • STEARIC ACID (UNII: 4ELV7Z65AP)
  • TRIETHOXYCAPRYLYLSILANE (UNII: LDC331P08E)
  • COCO-CAPRYLATE/CAPRATE (UNII: 8D9H4QU99H)
  • DIMETHICONE (UNII: 92RU3N3Y1O)
  • ALKYL (C12-15) BENZOATE (UNII: A9EJ3J61HQ)
  • VINYL DIMETHICONE/METHICONE SILSESQUIOXANE CROSSPOLYMER (UNII: 9NH1UDD2RR)
  • PROPYLENE CARBONATE (UNII: 8D08K3S51E)
  • FERRIC OXIDE YELLOW (UNII: EX438O2MRT)
  • NEOPENTYL GLYCOL DIETHYLHEXANOATE (UNII: U68ZV6W62C)
  • .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
  • ADENOSINE (UNII: K72T3FS567)
  • FERRIC OXIDE RED (UNII: 1K09F3G675)
  • EDETATE DISODIUM ANHYDROUS (UNII: 8NLQ36F6MM)
  • CAMELLIA JAPONICA SEED OIL (UNII: U37N0S910T)
  • D&C RED NO. 33 (UNII: 9DBA0SBB0L)
  • NELUMBO NUCIFERA FLOWER (UNII: 61W322NLDV)
  • LONICERA JAPONICA FLOWER (UNII: 4465L2WS4Y)
  • STYPHNOLOBIUM JAPONICUM FLOWER (UNII: 644C3CSB6E)
  • SAFFLOWER (UNII: 4VBL71TY4Y)
  • CAMELLIA JAPONICA FLOWER (UNII: KUB8101TNF)
  • PRUNUS MUME FLOWER (UNII: 2N8872050J)
  • PYRUS COMMUNIS FLOWER (UNII: P6Y3X4TOIW)

Administration Route(s)

What are the Administration Route(s)?
The translation of the route code submitted by the firm, indicating route of administration.

  • Topical - Administration to a particular spot on the outer surface of the body. The E2B term TRANSMAMMARY is a subset of the term TOPICAL.

Product Labeler Information

What is the Labeler Name?
Name of Company corresponding to the labeler code segment of the Product NDC.

Labeler Name: Activebeuty Co.,ltd
Labeler Code: 73016
FDA Application Number: part352 What is the FDA Application Number?
This corresponds to the NDA, ANDA, or BLA number reported by the labeler for products which have the corresponding Marketing Category designated. If the designated Marketing Category is OTC Monograph Final or OTC Monograph Not Final, then the Application number will be the CFR citation corresponding to the appropriate Monograph (e.g. “part 341”). For unapproved drugs, this field will be null.

Marketing Category: OTC MONOGRAPH NOT FINAL - A product marketed pursuant to an Over-the-Counter (OTC) Drug Monograph that is not final. What is the Marketing Category?
Product types are broken down into several potential Marketing Categories, such as NDA/ANDA/BLA, OTC Monograph, or Unapproved Drug. One and only one Marketing Category may be chosen for a product, not all marketing categories are available to all product types. Currently, only final marketed product categories are included. The complete list of codes and translations can be found at www.fda.gov/edrls under Structured Product Labeling Resources.

Start Marketing Date: 04-03-2019 What is the Start Marketing Date?
This is the date that the labeler indicates was the start of its marketing of the drug product.

Listing Expiration Date: 12-31-2020 What is the Listing Expiration Date?
This is the date when the listing record will expire if not updated or certified by the product labeler.

Exclude Flag: N What is the NDC Exclude Flag?
This field indicates whether the product has been removed/excluded from the NDC Directory for failure to respond to FDA’s requests for correction to deficient or non-compliant submissions. Values = ‘Y’ or ‘N’.

* Please review the disclaimer below.

Actibeau Camellia Natural Mineral Uv Defense Sunscreen Product Label Images

Actibeau Camellia Natural Mineral Uv Defense Sunscreen Product Labeling Information

The product labeling information includes all published material associated to a drug. Product labeling documents include information like generic names, active ingredients, ingredient strength dosage, routes of administration, appearance, usage, warnings, inactive ingredients, etc.

Product Labeling Index

Otc - Active Ingredient

Zinc Oxide 10.952%


Titanium Dioxide 4.8184%

Otc - Purpose

Sunscreen

Indications & Usage

Helps prevent sunburn

Dosage & Administration

Apply liberally 15 minutes before sun exposure. Reapply at least every two hours

Warnings

For external use only.


Do not use on damaged or broken skin.


When using this product, keep out of eyes. Rinse with water to remove.


Stop using and ask a doctor if rash occurs.

Otc - Keep Out Of Reach Of Children

Keep out of reach of the children. If product is swallowed, get medical help or contact a poison control center right away.

Inactive Ingredient

WATER, CYCLOPENTASILOXANE, CAPRYLIC/CAPRIC TRIGLYCERIDE, BUTYLENE GLYCOL, ETHYLHEXYL PALMITATE, COCOS NUCIFERA (COCONUT) OIL, CETYL PEG/PPG-10/1 DIMETHICONE, DICAPRYLYL CARBONATE, NIACINAMIDE, ISOPROPYL MYRISTATE, GLYCERIN, 1,2-HEXANEDIOL, SODIUM CHLORIDE, CAPRYLYL METHICONE, QUATERNIUM-18 HECTORITE, EUPHORBIA CERIFERA (CANDELILLA) WAX, DIMETHICONE CROSSPOLYMER, ALUMINUM HYDROXIDE, BORON NITRIDE, PENTAERYTHRITYL TETRAETHYLHEXANOATE, SORBITAN ISOSTEARATE, POLYHYDROXYSTEARIC ACID, STEARIC ACID, TRIETHOXYCAPRYLYLSILANE, COCO-CAPRYLATE/CAPRATE, FRAGRANCE, DIMETHICONE, C12-15 ALKYL BENZOATE, VINYL DIMETHICONE/METHICONE SILSESQUIOXANE CROSSPOLYMER, PROPYLENE CARBONATE, FERRIC OXIDE YELLOW (CI 77492), NEOPENTYL GLYCOL DIETHYLHEXANOATE, TOCOPHERYL ACETATE, DIMETHICONE/PEG-10/15 CROSSPOLYMER, ADENOSINE, FERRIC OXIDE RED (CI 77491), DISODIUM EDTA, CAMELLIA JAPONICA SEED OIL, D&C RED NO. 33 (CI 17200), NELUMBO NUCIFERA FLOWER EXTRACT, LONICERA JAPONICA (HONEYSUCKLE) FLOWER EXTRACT, SOPHORA JAPONICA FLOWER EXTRACT, CARTHAMUS TINCTORIUS (SAFFLOWER) FLOWER EXTRACT, CAMELLIA JAPONICA FLOWER EXTRACT, PRUNUS MUME FLOWER EXTRACT, PYRUS COMMUNIS (PEAR) FLOWER EXTRACT

* Please review the disclaimer below.

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