NDC 43948-6001 High Protection Sun Air Spray Spf50 Pa

NDC Product Code 43948-6001

NDC 43948-6001-1

Package Description: 130 mL in 1 BOTTLE, SPRAY

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

NDC Product Information

High Protection Sun Air Spray Spf50 Pa with NDC 43948-6001 is a product labeled by The Doctor's Cosmetic Inc. The generic name of High Protection Sun Air Spray Spf50 Pa is . The product's dosage form is and is administered via form.

Labeler Name: The Doctor's Cosmetic Inc

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.


Product Labeler Information

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

Labeler Name: The Doctor's Cosmetic Inc
Labeler Code: 43948
Start Marketing Date: 11-01-2009 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.

High Protection Sun Air Spray Spf50 Pa Product Label Images

High Protection Sun Air Spray Spf50 Pa 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

Inactive Ingredient

INACTIVE INGREDIENTS:Water, Cyclopentasiloxane, Ethylhexyl Methosycinnamate, Alcohol, Zinc Oxide, Ethylhexyl Salicylate, Isodecyl Neopentanoate, Butylene Glycol, Titanium Dioxide, Peg-10 Dimethicone, Methyl Methacrylate Crosspolymer, Methicone, Aluminum Stearate, Aluminum Hydroxide, Sodium Chloride, Fragrance, Calcium Aluminum Borosilicate, Imidazolidinyl Urea, Polyglyceryl-6 Polyricinoleate, Sodium Hyaluronate, Rosemarinus Officinalis (Rosemary) Leaf Extract, Opuntia Ficus - Indica Extract, Chamomilla Recutita (Matricaria) Flower Extract, Aloe Barbadensis Leaf Juice, Methylparaben, Propylparaben, Butylparaben

Otc - Keep Out Of Reach Of Children

CAUTION: Keep away from children.

Otc - When Using

DIRECTION OF USE:Apply 15-30 minutes before sun exposure.  Do not apply in windy conditions.  Hold can 4-6 inches away from body and apply liberally, spraying slowly and evenly until product is visible on skin.  Spray into hand and apply to the face.  Use in well ventilated areas.  Reapply after swimming, excessive perspiration, towel drying or extended sun exposure.

* Please review the disclaimer below.