NDC 59663-001 Moisturizing Sunscreen Spf15

NDC Product Code 59663-001

NDC CODE: 59663-001

Proprietary Name: Moisturizing Sunscreen Spf15 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.

NDC Code Structure

  • 59663 - Shine & Pretty (usa), Corp.

NDC 59663-001-01

Package Description: 100 mL in 1 BOTTLE

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.

NDC Product Information

Moisturizing Sunscreen Spf15 with NDC 59663-001 is a product labeled by Shine & Pretty (usa), Corp.. The product's dosage form is and is administered via form.

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.

  • SORBITAN SESQUIOLEATE (UNII: 0W8RRI5W5A)
  • POLYSORBATE 60 (UNII: CAL22UVI4M)
  • CARBOMER 934 (UNII: Z135WT9208)
  • VITAMIN E ACETATE (UNII: 9E8X80D2L0)
  • STEARIC ACID (UNII: 4ELV7Z65AP)
  • PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
  • VITAMIN A PALMITATE (UNII: 1D1K0N0VVC)
  • PROPYLPARABEN (UNII: Z8IX2SC1OH)
  • TROLAMINE (UNII: 9O3K93S3TK)
  • GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)
  • ALOE VERA LEAF (UNII: ZY81Z83H0X)
  • WATER (UNII: 059QF0KO0R)
  • DIAZOLIDINYL UREA (UNII: H5RIZ3MPW4)
  • ETHYLHEXYL PALMITATE (UNII: 2865993309)
  • ALUMINUM STARCH OCTENYLSUCCINATE (UNII: I9PJ0O6294)
  • METHYLPARABEN (UNII: A2I8C7HI9T)
  • CHAMAEMELUM NOBILE FLOWER (UNII: O2T154T6OG)

Product Labeler Information

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

Labeler Name: Shine & Pretty (usa), Corp.
Labeler Code: 59663
Start Marketing Date: 02-02-1996 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: 12-31-2017 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: I - INACTIVATED, the listing data was inactivated by the FDA. 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.

Moisturizing Sunscreen Spf15 Product Label Images

Moisturizing Sunscreen Spf15 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 - Purpose

For Sun protection: Apply on surfaces of skin, on face, arm and hand. SPF-15 provides the face and body skin with effective protection against harmful UVA and UVB rays. Use daily over moisture cream to help prevent premature aging and wrinkling due to prolonged exposure to the sun, reapply after swimming or excessive exercise.

Indications & Usage

Smear Lightly.

Warnings

Warning: For external use only, not to be swallowed. Avoid contact with eye. Discontinue if signs of irritation or rash appear.

Dosage & Administration

To Apply lightly.

Inactive Ingredient

Inactive Ingredients: SORBITAN SESQUIOLEATE, POLYSORBATE 60, CARBOMER 934, VITAMIN E ACETATE, STEARIC ACID, PROPYLENE GLYCOL, VITAMIN A PALMITATE, PROPYLPARABEN, Water.

Otc - Keep Out Of Reach Of Children

Keep Out of the reach of children. Use on children under six months of age only with the advice of a physician.

Otc - Active Ingredient

OXYBENZONE and OCTINOXATE.

* Please review the disclaimer below.