NDC 65364-220 Kiss My Face Spf 30 Lip Balm

Product Information

Kiss My Face Spf 30 Lip Balm is product labeled by Kiss My Face. The product's dosage form is and is administered via form.

Product Code65364-220
Proprietary Name 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.
Kiss My Face Spf 30 Lip Balm
Product Labeler Information What is the Labeler Name?
Name of Company corresponding to the labeler code segment of the Product NDC.
Kiss My Face
Labeler Code65364
Start Marketing Date 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 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 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".
NDC Code Structure

What are the uses for Kiss My Face Spf 30 Lip Balm?

Product Characteristics

Color(s)WHITE (C48325)

Product Packages

NDC 65364-220-01

Package Description: 1 g in 1 CONTAINER

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

Product Details

Kiss My Face Spf 30 Lip Balm Active Ingredients UNII Codes

Kiss My Face Spf 30 Lip Balm Inactive Ingredients UNII Codes

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.

* Please review the disclaimer below.

Kiss My Face Spf 30 Lip Balm Labeling and Warnings

FDA filings in the form of structured product labels are documents that include all published material associated whith this product. Product label information includes data like indications and usage generic names, contraindications, active ingredients, strength dosage, routes of administration, appearance, usage, warnings, inactive ingredients, etc.

Table of Contents

Active Ingredient

Avobenzone (3.0%), Homosalate (8.0%), Octinoxate (7.0%), Octocrylene (2.0%)



Keep Out Of Reach Of Children

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


Helps prevent sunburn.


For external use only. 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 occurs.


Apply liberally 15 minutes before sun exposure. Reapply: after 80 minutes of swimming or sweating, immediately after towel drying, at least every 2 hours. Sun Protection Measures: Spending time in the sun increases your risk of skin cancer and early skin aging. To decrease the risk, regularly use a sunscreen with a Broad Spectrum SPF of 15 or higher and other sun protection measures including: Limit time in the sun, especially from 10 AM – 2 PM . Wear long-sleeved shirts, pants, hats and sunglasses. Children under 6 months: Ask a doctor.

Inactive Ingredients

Aloe Barbadensis Leaf Extract*, Butyrospermum Parkii (Shea Butter), Calendula Officinalis Flower Extract*, Beeswax*, Cocos Nucifera (Coconut) Oil*, Cucumis Sativus (Cucumber) Fruit Extract*, Geranium Maculatum Extract*, Hippophae Rhamnoides Oil, Lecithin*, Pelargonium Graveolens Flower Oil Rosa Canina, Extract*,Sambucus Nigra Flower Extract*,


* Please review the disclaimer below.