NDC 71454-1038 Herbaid Acne Relief Body Cleanser

Salicylic Acid

NDC Product Code 71454-1038

NDC Code: 71454-1038

Proprietary Name: Herbaid Acne Relief Body Cleanser 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: Salicylic Acid 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

  • 71454 - Gc Us Corporation
    • 71454-1038 - Herbaid Acne Relief Body Cleanser

NDC 71454-1038-2

Package Description: 1 BOTTLE, PLASTIC in 1 CASE > 320 mL in 1 BOTTLE, PLASTIC

NDC Product Information

Herbaid Acne Relief Body Cleanser with NDC 71454-1038 is a a human over the counter drug product labeled by Gc Us Corporation. The generic name of Herbaid Acne Relief Body Cleanser is salicylic acid. The product's dosage form is liquid and is administered via topical form.

Labeler Name: Gc Us Corporation

Dosage Form: Liquid - A dosage form consisting of a pure chemical in its liquid1 state. This dosage form term should not be applied to solutions.

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.

Herbaid Acne Relief Body Cleanser 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.

  • SALICYLIC ACID 1.6 g/320mL

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.

  • URTICA DIOICA LEAF (UNII: X6M0DRN46Q)
  • CITRUS JUNOS FRUIT (UNII: 53KHW58C1V)
  • GLYCERIN (UNII: PDC6A3C0OX)
  • DECYL GLUCOSIDE (UNII: Z17H97EA6Y)
  • COCOYL METHYL MONOETHANOLAMINE (UNII: 79G1T427CF)
  • DISODIUM COCOAMPHODIACETATE (UNII: 18L9G3U51M)
  • COCO-BETAINE (UNII: 03DH2IZ3FY)
  • LEMON (UNII: 24RS0A988O)
  • ALOE VERA LEAF (UNII: ZY81Z83H0X)
  • LACTIC ACID (UNII: 33X04XA5AT)
  • BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
  • ORANGE (UNII: 5EVU04N5QU)
  • CAULERPA LENTILLIFERA (UNII: VJ0188QOU3)
  • LAVANDULA ANGUSTIFOLIA SUBSP. ANGUSTIFOLIA FLOWER (UNII: 19AH1RAF4M)
  • MONARDA DIDYMA LEAF (UNII: JY15982UBB)
  • MENTHA PIPERITA LEAF (UNII: A389O33LX6)
  • MATRICARIA CHAMOMILLA FLOWERING TOP (UNII: 3VNC7T6Z02)
  • CHAMOMILE (UNII: FGL3685T2X)
  • ROSEMARY (UNII: IJ67X351P9)
  • GRAPEFRUIT (UNII: O82C39RR8C)
  • WATER (UNII: 059QF0KO0R)
  • CARROT (UNII: L56Z1JK48B)
  • TOMATO (UNII: Z4KHF2C175)
  • EUCALYPTUS OIL (UNII: 2R04ONI662)
  • HAMAMELIS VIRGINIANA LEAF (UNII: T07U1161SV)
  • CELERY (UNII: 44IDY6DTKX)
  • RICE GERM (UNII: 7N2B70SFEZ)
  • TRICHOLOMA MAGNIVELARE WHOLE (UNII: 9BMU5DJ83C)
  • POTATO PULP (UNII: 844I2DX0IS)
  • CABBAGE (UNII: GW0W1Y9I97)
  • COPAIFERA OFFICINALIS RESIN (UNII: 1VH544O5AT)
  • ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
  • HYDROXYACETOPHENONE (UNII: G1L3HT4CMH)
  • PENTYLENE GLYCOL (UNII: 50C1307PZG)
  • CAPRYLYL GLYCOL (UNII: 00YIU5438U)
  • CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
  • EUCALYPTUS GLOBULUS LEAF (UNII: S546YLW6E6)
  • CLOVE (UNII: K48IKT5321)
  • SCUTELLARIA BAICALENSIS ROOT (UNII: 7J95K7ID2S)
  • KALE (UNII: 0Y3L4J38H1)
  • REISHI (UNII: TKD8LH0X2Z)
  • ORANGE OIL (UNII: AKN3KSD11B)
  • LAVENDER OIL (UNII: ZBP1YXW0H8)
  • PELARGONIUM GRAVEOLENS FLOWER OIL (UNII: 3K0J1S7QGC)
  • TETRADECENE (UNII: FW23481S7S)
  • HEXADECENE (MIXED ISOMERS) (UNII: 38H8547VP0)
  • SODIUM SULFATE (UNII: 0YPR65R21J)
  • SODIUM CHLORIDE (UNII: 451W47IQ8X)
  • HEXYLENE GLYCOL (UNII: KEH0A3F75J)
  • LOWBUSH BLUEBERRY (UNII: G90PX41VP0)
  • CHAMAEMELUM NOBILE FLOWER (UNII: O2T154T6OG)
  • CALENDULA OFFICINALIS FLOWER (UNII: P0M7O4Y7YD)
  • THYME (UNII: CW657OBU4N)
  • TANACETUM PARTHENIUM (UNII: 6GE7Z0761K)
  • ALOYSIA CITRODORA LEAF (UNII: 9B1F4HKA9O)
  • BELLIS PERENNIS FLOWER (UNII: 26I94X9A1K)
  • OREGANO (UNII: 0E5AT8T16U)
  • SAGE (UNII: 065C5D077J)
  • SODIUM C14-16 OLEFIN SULFONATE (UNII: O9W3D3YF5U)
  • POLYQUATERNIUM-10 (1000 MPA.S AT 2%) (UNII: GMR4PEN8PK)
  • SELAGINELLA LEPIDOPHYLLA (UNII: 02JQ564P1G)
  • FREESIA ALBA FLOWER (UNII: 33X293N6JT)
  • BROCCOLI (UNII: UOI4FT57BZ)
  • MELALEUCA ALTERNIFOLIA LEAF (UNII: G43C57162K)
  • PHELLINUS LINTEUS WHOLE (UNII: YVO92B1UCA)
  • CUPRIC CATION (UNII: 8CBV67279L)
  • SODIUM METHYL COCOYL TAURATE (UNII: JVL98CG53G)
  • BERGAMOT OIL (UNII: 39W1PKE3JI)
  • 1,2-HEXANEDIOL (UNII: TR046Y3K1G)

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: Gc Us Corporation
Labeler Code: 71454
FDA Application Number: part333D 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 FINAL - A product marketed pursuant to a final Over-the-Counter (OTC) Drug Monograph. 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: 06-20-2019 What is the Start Marketing Date?
This is the date that the labeler indicates was the start of its marketing of the drug product.

End Marketing Date: 12-31-2030 What is the End Marketing Date?
This is the date the product will no longer be available on the market. If a product is no longer being manufactured, in most cases, the FDA recommends firms use the expiration date of the last lot produced as the EndMarketingDate, to reflect the potential for drug product to remain available after manufacturing has ceased. Products that are the subject of ongoing manufacturing will not ordinarily have any EndMarketingDate. Products with a value in the EndMarketingDate will be removed from the NDC Directory when the EndMarketingDate is reached.

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.

Information for Patients

Salicylic Acid Topical

Salicylic Acid Topical is pronounced as (sal'' i sil' ik as' id)

Why is salicylic acid topical medication prescribed?
Topical salicylic acid is used to help clear and prevent pimples and skin blemishes in people who have acne. Topical salicylic acid is also used to treat skin conditions ...
[Read More]

* Please review the disclaimer below.

Herbaid Acne Relief Body Cleanser Product Label Images

Herbaid Acne Relief Body Cleanser 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

Active Ingredients

Salicylic Acid 0.5%

Otc - Purpose

Sunscreen

Uses

  • For the treatment of acne.

Warnings

Warnings: For external use only.

When using this product skin irritation and dryness is more likely to occur if you use another topical acne medication at the same time. If irritation occurs, only use one topical acne medication at a time. avoid contact with eyes. If contact occurs, flush thoroughly with water.

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

Do Not Use

On damaged or broken skin.

When Using This Product

Keep out of eyes. Rinse with water to remove.

Stop Use And Ask A Doctor If

Rash or irritation develops and lasts

Keep Out Of Reach Of Children.

If swallowed, get medical help or contact a Poison Control Center right away.

Directions

  • Use daily in the shower or bathfor maximum lather, massage over wet skin with a washcloth or body puff, concentrating on areas prone to breakouts.rinse well.

Other Information

  • Store at room temperature.

Inactive Ingredients

Water, Sodium C14-16 Olefin Sulfonate, Glycerin, Decyl Glucoside, Cocamide Methyl MEA, Disodium Cocoamphodiacetate, Coco-Betaine, Sodium Methyl Cocoyl Taurate, Polyquaternium-10, Lactic Acid, Butylene Glycol, Selaginella Lepidophylla Extract, Caulerpa Lentillifera Extract, Lavandula Angustifolia (Lavender) Flower Extract, Monarda Didyma Leaf Extract, Mentha Piperita (Peppermint) Leaf Extract, Freesia Refracta Extract, Chamomilla Recutita (Matricaria) Flower Extract, Rosmarinus Officinalis (Rosemary) Leaf Extract, Brassica Oleracea Italica (Broccoli) Extract, Daucus Carota Sativa (Carrot) Root Extract, Solanum Lycopersicum (Tomato) Fruit Extract, Vaccinium Angustifolium (Blueberry) Fruit Extract, Anthemis Nobilis Flower Extract, Calendula Officinalis Flower Extract, Thymus Vulgaris (Thyme) Extract, Chrysanthemum Parthenium (Feverfew) Extract, Lippia Citriodora Leaf Extract, Bellis Perennis (Daisy) Flower Extract, Origanum Vulgare Leaf Extract, Salvia Officinalis (Sage) Leaf Extract, Urtica Dioica (Nettle) Extract, Melaleuca Alternifolia (Tea Tree) Extract, Hamamelis Virginiana (Witch Hazel) Leaf Extract, Citrus Limon (Lemon) Fruit Extract, Aloe Barbadensis Leaf Extract, Citrus Aurantium Dulcis (Orange) Fruit Extract, Chamomilla Recutita (Matricaria) Flower/Leaf Extract, Citrus Paradisi (Grapefruit) Fruit Extract, Citrus Junos Fruit Extract, Eucalyptus Globulus Leaf Extract, Eugenia Caryophyllus (Clove) Flower Extract, Scutellaria Baicalensis Root Extract, Apium Graveolens (Celery) Extract, Oryza Sativa (Rice) Extract, Brassica Oleracea Acephala Leaf Extract, Solanum Tuberosum (Potato) Pulp Extract, Phellinus Linteus Extract, Ganoderma Lucidum (Mushroom) Extract, Tricholoma Matsutake Extract, Brassica Oleracea Capitata (Cabbage) Leaf Extract, Citrus Aurantium Bergamia (Bergamot) Fruit Oil, Citrus Aurantium Dulcis (Orange) Peel Oil, Lavandula Angustifolia (Lavender) Oil, Copaifera Officinalis (Balsam Copaiba) Resin, Eucalyptus Globulus Leaf Oil, Pelargonium Graveolens Flower Oil, 1,2-Hexanediol, Ethylhexylglycerin, Tetradecene, Hexadecene, Sodium Sulfate, Sodium Chloride, Hexylene Glycol, Disodium EDTA, Hydroxyacetophenone, Pentylene Glycol, Caprylyl Glycol, Citric Acid

Questions?

  • Side effects occur. You may report side effects to FDA at 1-800-FDA-1088.

Accessories

Net Wt. 10.82oz/320mlManufactured for Woosincosmetics Inc.140, Nae-dong, Ojeong-gu, Bucheon-si, Gyeonggi-do, Korea 14491MADE IN KOREA/Fabriqué en Corée

* Please review the disclaimer below.

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