NDC 68814-250 Skin Firm Lipoamino Hydrator Spf 15 Molton Brown

  1. Labeler Index
  2. Molton Brown Ltd
  3. NDC: 68814-250 Skin Firm Lipoamino Hydrator Spf 15 Molton Brown

NDC Product Code 68814-250

NDC CODE: 68814-250

Proprietary Name: Skin Firm Lipoamino Hydrator Spf 15 Molton Brown 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: 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

  • 68814 - Molton Brown Ltd
    • 68814-250 - Skin Firm Lipoamino Hydrator Spf 15

NDC 68814-250-02

Package Description: 1 BOTTLE in 1 CARTON > 50 mL in 1 BOTTLE (68814-250-01)

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

NDC Product Information

Skin Firm Lipoamino Hydrator Spf 15 Molton Brown with NDC 68814-250 is a product labeled by Molton Brown Ltd. The generic name of Skin Firm Lipoamino Hydrator Spf 15 Molton Brown is . The product's dosage form is and is administered via form.

Labeler Name: Molton Brown Ltd

Dosage Form: -

Product Type: 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.

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)
  • COCONUT ALKANES (UNII: 1E5KJY107T)
  • ENSULIZOLE (UNII: 9YQ9DI1W42)
  • ALKYL (C12-15) BENZOATE (UNII: A9EJ3J61HQ)
  • GLYCERIN (UNII: PDC6A3C0OX)
  • OLIVE OIL (UNII: 6UYK2W1W1E)
  • SHEA BUTTER (UNII: K49155WL9Y)
  • CHAMAECYPARIS OBTUSA WOOD OIL (UNII: P2OMP71Y62)
  • LONICERA CAPRIFOLIUM FLOWER (UNII: 5N1WD9784U)
  • LONICERA JAPONICA FLOWER (UNII: 4465L2WS4Y)
  • HYALURONATE SODIUM (UNII: YSE9PPT4TH)
  • COCO-CAPRYLATE/CAPRATE (UNII: 8D9H4QU99H)
  • DIPALMITOYL HYDROXYPROLINE (UNII: E6AHA53N1H)
  • SODIUM ACRYLATE/SODIUM ACRYLOYLDIMETHYLTAURATE COPOLYMER (4000000 MW) (UNII: 1DXE3F3OZX)
  • ISOHEXADECANE (UNII: 918X1OUF1E)
  • POLYSORBATE 80 (UNII: 6OZP39ZG8H)
  • SORBITAN MONOOLEATE (UNII: 06XEA2VD56)
  • CETEARYL OLIVATE (UNII: 58B69Q84JO)
  • SORBITAN OLIVATE (UNII: MDL271E3GR)
  • SORBITAN MONOPALMITATE (UNII: 77K6Z421KU)
  • CETYL PALMITATE (UNII: 5ZA2S6B08X)
  • CARBOMER 934 (UNII: Z135WT9208)
  • .ALPHA.-TOCOPHEROL (UNII: H4N855PNZ1)
  • PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
  • PHENOXYETHANOL (UNII: HIE492ZZ3T)
  • METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)
  • TROLAMINE (UNII: 9O3K93S3TK)
  • CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)

Product Labeler Information

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

Labeler Name: Molton Brown Ltd
Labeler Code: 68814
Start Marketing Date: 09-01-2011 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 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.

Skin Firm Lipoamino Hydrator Spf 15 Molton Brown Product Label Images

Skin Firm Lipoamino Hydrator Spf 15 Molton Brown 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      Purpose

Avobenzone 3%           SunscreenEnsulizole 1%               SunscreenOctinoxate 5%             SunscreenOctocrylene 2%            Sunscreen

Use

UseProvides medium protection against sunburnFor skin highly sensitive to sunburn

Warning

Keep out of reach of children

Indications

Stop use and ask a doctor if skin rash or irritation occurs

Warnings

For external use onlySun alert: Limiting sun exposure, wearing protective clothing and using sunscreens may reduce the risk of skin ageing, skin cancer, and other harmful effects of the sun.  When using this product: Keep out of eyes. Rinse with water to remove. If swallowed, get medical help or contact a poison control center right away.

Directions

Apply a small amount to your face and neck, morning and evening, after washing and shaving.

Inactive Ingredients

Water, coconut alkanes, nylon 6/12, C12-15 alkyl benzoate, glycerin, olea europaea (olive) fruit oil, butyrospermum parkii (shea) butter, fragrance, chamaecyparis obtusa oil, lonicera caprifolium (honeysuckle) flower extract, lonicera japonica (honeysuckle) flower extract, sodium hyaluronate, coco-caprylate/caprate, dipalmitoyl hydroxyproline, sodium acrylate/sodium acryloyldimethyl taurate copolymer, isohexadecane, polysorbate 80, sorbitan oleate, cetearyl olivate, sorbitan palmitate, cetyl palmitate, carbomer, tocopherol, propylene glycol, phenoxyethanol, methylisothiazolinone, thriethanolamine, citric acid.

* Please review the disclaimer below.