NDC 81883-101 Mineral Sunscreen Spf 30

Zinc Oxide

NDC Product Information

Mineral Sunscreen Spf 30 with NDC 81883-101 is a a human over the counter drug product labeled by Taos Aer Llc. The generic name of Mineral Sunscreen Spf 30 is zinc oxide. The product's dosage form is lotion and is administered via topical form.

Dosage Form: Lotion - An emulsion, liquid1 dosage form. This dosage form is generally for external application to the skin.2

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.

Mineral Sunscreen Spf 30 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.


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.

  • OLIVE OIL (UNII: 6UYK2W1W1E)
  • SAGE OIL (UNII: U27K0H1H2O)
  • LIMONENE, (+)- (UNII: GFD7C86Q1W)
  • LINALOOL, (+)- (UNII: F4VNO44C09)
  • VETIVER OIL (UNII: 9M9P32M01L)
  • JUNIPERUS VIRGINIANA OIL (UNII: PAD4FN7P2G)
  • BERGAMOT OIL (UNII: 39W1PKE3JI)
  • MARITIME PINE (UNII: 50JZ5Z98QY)
  • POMEGRANATE SEED OIL (UNII: 0UI45XV0T6)
  • ALOE VERA LEAF (UNII: ZY81Z83H0X)
  • PANTHENOL (UNII: WV9CM0O67Z)
  • XANTHAN GUM (UNII: TTV12P4NEE)
  • PHENYLETHYL ALCOHOL (UNII: ML9LGA7468)
  • PENTYLENE GLYCOL (UNII: 50C1307PZG)
  • PROPANEDIOL (UNII: 5965N8W85T)
  • LAUROYL LYSINE (UNII: 113171Q70B)
  • MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U)
  • SORBITAN OLIVATE (UNII: MDL271E3GR)
  • WATER (UNII: 059QF0KO0R)
  • SUNFLOWER OIL (UNII: 3W1JG795YI)
  • GLYCERIN (UNII: PDC6A3C0OX)
  • SQUALANE (UNII: GW89575KF9)
  • DICAPRYLYL CARBONATE (UNII: 609A3V1SUA)
  • CETEARYL OLIVATE (UNII: 58B69Q84JO)
  • SHEA BUTTER ETHYL ESTERS (UNII: V2CI786FPG)
  • SORBITAN SESQUIOLEATE (UNII: 0W8RRI5W5A)
  • DIGLYCERIN (UNII: 3YC120743U)
  • POLYHYDROXYSTEARIC ACID (2300 MW) (UNII: YXH47AOU0F)

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: Taos Aer Llc
Labeler Code: 81883
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: 09-18-2021 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 - NO 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.

Mineral Sunscreen Spf 30 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 Ingredient

ZINC OXIDE 20%

Purpose

SUNSCREEN

Uses

  • HELPS PREVENT SUNBURNIF USED AS DIRECTED WITH OTHER SUN PROTECTION MEASURE (SEE DIRECTIONS), DECREASES THE RISK OF SKIN CANCER AND EARLY SKIN AGING CAUSED BY THE SUN

Warnings

  • 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 SWALLOWED, GET MEDICAL HELP OR CONTACT POISON CONTROL CENTER RIGHT AWAY.

Directions

  • SHAKE WELL. APPLY AT LEAST 1 PUMP TO FACE. APPLY ADDITIONAL PUMPS TO NECK AND CHEST - AREAS THAT ARE OFTEN IGNORED.APPLY LIBERALLY 15 MINUTES BEFORE SUN EXPOSURE.REAPPLY EVERY 2 HOURSSUN PROTECTION MEASURES: SPENDING TIME IN THE SUN INCREASES YOUR RISK OF SKIN CANCER AND EARLY SKIN AGING. TO DECREASE THIS 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 BETWEEN 10 A.M. AND 2 P.M. WEAR LONG-SLEEVED SHIRTS, PANTS, HATS AND SUNGLASSESCHILDREN UNDER 6 MONTHS: CONSULT A PHYSICIAN

Inactive Ingredients

WATER (AQUA), HELIANTHUS ANNUUS (SUNFLOWER) SEED OIL, CAPRYLIC/CAPRIC TRIGLYCERIDE, OLEA EUROPEA (OLIVE FRUIT) OIL, DICAPRYL CARBONATE, CETEARYL OLIVATE, SORBITAN OLIVATE, GLYCERIN, SHEA BUTTER CETYL ESTERS, SORBITAN SESQUIOLEATE, POLYHYDROXYSTEARIC ACID, DIGLYCERIN, PINUS PINASTER (CLUSTER PINE) BARK EXTRACT, PUNICA GRANATUM (POMEGRANATE) SEED OIL, PHENETHYL ALCOHOL, PENTYLENE GLYCOL, PROPANEDIOL, ALOE BARBADENSIS (ALOE VERA) LEAF JUICE POWDER, PANTHENOL, XANTHAN GUM, LAUROYL LYSINE, VETIVERIA ZIZANOIDES (VETIVER) ROOT OIL, JUNIPERUS VIRGINIANA (CEDAR) WOOD OIL, CITRUS AURANTIUM BERGAMIA (BERGAMOT) FRUIT OIL, SALVIA OFFICINALIS (SAGE) OIL, LIMONENE-D, LINALOOL

Other Information

PROTECT THIS PRODUCT AWAY FROM EXCESSIVE HEAT AND DIRECT SUNLIGHT. STORE BELOW 90°F (32°C). MAY STAIN SOME FABRICS.

* Please review the disclaimer below.