NDC 64942-1858 Mele Men Plus Care Hydrate Face

No Shade Sunscreen Oil

NDC Product Code 64942-1858

NDC 64942-1858-2

Package Description: 1 BOTTLE, DROPPER in 1 CARTON > 29.57 mL in 1 BOTTLE, DROPPER (64942-1858-1)

NDC Product Information

Mele Men Plus Care Hydrate Face with NDC 64942-1858 is a a human over the counter drug product labeled by Conopco Inc. D/b/a Unilever. The generic name of Mele Men Plus Care Hydrate Face is no shade sunscreen oil. The product's dosage form is oil and is administered via topical form.

Labeler Name: Conopco Inc. D/b/a Unilever

Dosage Form: Oil - An unctuous, combustible substance which is liquid, or easily liquefiable, on warming, and is soluble in ether but insoluble in water. Such substances, depending on their origin, are classified as animal, mineral, or vegetable oils.

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.

Mele Men Plus Care Hydrate Face 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.

  • OCTINOXATE 7.49 g/100mL
  • AVOBENZONE 2 g/100mL

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.

  • LIMONENE, (+)- (UNII: GFD7C86Q1W)
  • LINALOOL, (+/-)- (UNII: D81QY6I88E)

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: part352 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 NOT FINAL - A product marketed pursuant to an Over-the-Counter (OTC) Drug Monograph that is not final. 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: 02-12-2021 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 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.

Mele Men Plus Care Hydrate Face Product Label Images

Mele Men Plus Care Hydrate Face 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

Melē No Shade Sunscreen Oil Spf 30 - (Sunscreen, Avobenzone, Octinoxate) Oil

Melē No Shade Sunscreen Oil SPF 30

Drug Facts

Active ingredient
Avobenzone 3%

Octinoxate 7.49%




Help prevent sunburn

If used as directed with other sun protectionmeaseure (see Directions) decreases the risk of skin cancer and early skin aging caused by the sun


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

Otc - Keep Out Of Reach Of Children

Keep out of reach of children
If product is swallowed, get medical help or contact a PoisonCcontrol Center right away.


Apply to all skin exposed to the sun.

Apply liberally and evenly 15 minutes before sun exposure.

Reapply at least every 2 hours.

Use a water resistant sunscreen if swimming or sweating.

For children under 6 months of age. Ask a doctor.

Sun Protection Measures Spending time in the sun increases your risk of skin cancer and early skin aging. To decrease this rish, regularly use a sunscreen with a Broad Spectum SPF value of 15 or higher and other sun protection measures including
limit time in the sun, especiallu from 10a.m. - 2p.m. wear long-sleeved shirts, pants, hats and sunglasses

Other Information

Protect the product in this container from excessive heat and direct sun.

Inactive Ingredients

Octyldodecanol, Isohexadecane, Caprylic/Capric Triglyceride, C12-15 Alkyl Benzoate, Dimethicone, Butyloctyl Salicylate, Ethylcellulose, Fragrance (Parfum), Coumarin, Limonene, Linalool.

* Please review the disclaimer below.