NDC 64942-1861 St. Ives Blemish And Blackhead Control Apricot Scrub

Solutions Acne Control Spot Treatment

NDC Product Code 64942-1861

NDC CODE: 64942-1861

Proprietary Name: St. Ives Blemish And Blackhead Control Apricot Scrub 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: Solutions Acne Control Spot Treatment 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

  • 64942 - Conopco Inc. D/b/a Unilever

NDC 64942-1861-1

Package Description: 22 g in 1 TUBE

NDC Product Information

St. Ives Blemish And Blackhead Control Apricot Scrub with NDC 64942-1861 is a a human over the counter drug product labeled by Conopco Inc. D/b/a Unilever. The generic name of St. Ives Blemish And Blackhead Control Apricot Scrub is solutions acne control spot treatment. The product's dosage form is lotion and is administered via topical form. The RxNorm Crosswalk for this NDC code indicates a single RxCUI concept is associated to this product: 103568.

Dosage Form: Lotion - An emulsion, liquid1 dosage form. This dosage form is generally for external application to the skin.2

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.

St. Ives Blemish And Blackhead Control Apricot Scrub 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.


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)
  • GLYCERIN (UNII: PDC6A3C0OX)
  • MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U)
  • STEARETH-2 (UNII: V56DFE46J5)
  • MAGNESIUM ALUMINUM SILICATE (UNII: 6M3P64V0NC)
  • SHEA BUTTER (UNII: K49155WL9Y)
  • STEARETH-21 (UNII: 53J3F32P58)
  • CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
  • PHENOXYETHANOL (UNII: HIE492ZZ3T)
  • HYDROGENATED JOJOBA OIL, RANDOMIZED (UNII: Q47ST02F58)
  • MENTHOL (UNII: L7T10EIP3A)
  • XANTHAN GUM (UNII: TTV12P4NEE)
  • HELIANTHUS ANNUUS SEED WAX (UNII: 42DG15CHXV)
  • PHYTATE SODIUM (UNII: 88496G1ERL)
  • NIACINAMIDE (UNII: 25X51I8RD4)
  • POLYGLYCERIN-3 (UNII: 4A0NCJ6RD6)
  • ACACIA DECURRENS FLOWER WAX (UNII: AU6XZE9IY9)
  • BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
  • MELALEUCA ALTERNIFOLIA FLOWERING TOP (UNII: 5AZ4S6N66F)
  • HAMAMELIS VIRGINIANA LEAF (UNII: T07U1161SV)
  • POWDERED CELLULOSE (UNII: SMD1X3XO9M)

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: Conopco Inc. D/b/a Unilever
Labeler Code: 64942
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: 07-01-2021 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: 12-31-2022 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 - NO 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 ("Y"), or because the listing certification is expired ("E"), or because the listing data was inactivated by FDA ("I"). Values = "Y", "N", "E", or "I".

* Please review the disclaimer below.

St. Ives Blemish And Blackhead Control Apricot Scrub Product Label Images

St. Ives Blemish And Blackhead Control Apricot Scrub 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 Ingredient

Salicylic Acid (2%)

Purpose

Acne Treatment

Uses

For the mangement of acne

Helps prevent new acne pimples and acne blemishes from forming

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 occues, only use one topical acne medication at a time.

Otc - Keep Out Of Reach Of Children

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

Directions

Cleanse skin thoroughly before applying product

Cover the entire affected area with a thin layer one to three times daily

Because excessive drying of the skin may occur, start with one application daily, then gradually increase to two or three times daily, if needed or as directed by a doctor.

If bothersome dryness or peeling occurs, reduce application to once a day or every other day.

Other Information

Product contains menthol. If you experience discomfort, please stop use

Inactive Ingredients

Water (Aqua), Cellulose, Caprylic/Capric Triglyceride, Steareth-2, Glycerin, Magnesium Aluminum Silicate, Butyrospermum Parkii (Shea) Butter, Cetearyl Alcohol, Steareth-21, Phenoxyethanol, Jojoba Esters, Menthol, Xanthan Gum, Helianthus Annuus (Sunflower) Seed Wax, Sodium Phytate, Niacinamide, Polyglycerin-3, Acacia Decurrens Flower Wax, Tasmannia Lanceolata Fruit/Leaf Extract, Butylene Glycol, Hamamelis Virginiana (Witch Hazel) Leaf Extract, Melaleuca Alternifolia (Tea Tree) Flower/Leaf/Stem Extract.

* Please review the disclaimer below.