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Summers eve active chafe - Medication Information

Product NDC Code 0132-8744
Drug Name

Summers eve active chafe

Type Brand
Pharm Class Skin Barrier Activity [PE]
Active Ingredients
Dimethicone 12 mg/g
Route TOPICAL
Dosage Form GEL
RxCUI drug identifier 706952
Application Number part347
Labeler Name C.B. Fleet Company, Inc.
Packages
Package NDC Code Description
0132-8744-42 1 jar in 1 carton (0132-8744-42) / 42 g in 1 jar
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Active ingredient

A list of the active, medicinal ingredients in the drug product.
Active Ingredient

Dosage and administration

Information about the drug product’s dosage and administration recommendations, including starting dose, dose range, titration regimens, and any other clinically sigificant information that affects dosing recommendations.
Directions Apply as needed.

Inactive ingredient

A list of inactive, non-medicinal ingredients in a drug product.
Inactive Ingredients dimethicone, dimethicone/vinyl dimethicone crosspolymer, cyclopentasiloxane, vinyl dimethicone/methicone silsesquioxane crosspolymer, silica dimethyl silylate

Indications and usage

A statement of each of the drug products indications for use, such as for the treatment, prevention, mitigation, cure, or diagnosis of a disease or condition, or of a manifestation of a recognized disease or condition, or for the relief of symptoms associated with a recognized disease or condition. This field may also describe any relevant limitations of use.
Use Temporarily protects and helps relieve chafed, chapped, or cracked skin

Purpose

Information about the drug product’s indications for use.
Purpose Dimethicone 1.2%...................................Skin Protectant

Spl product data elements

Usually a list of ingredients in a drug product.
Summers Eve Active Chafe Dimethicone DIMETHICONE DIMETHICONE CYCLOMETHICONE 5 DIMETHICONE/VINYL DIMETHICONE CROSSPOLYMER (SOFT PARTICLE) SILICA DIMETHYL SILYLATE VINYL DIMETHICONE/METHICONE SILSESQUIOXANE CROSSPOLYMER

Package label principal display panel

The content of the principal display panel of the product package, usually including the product’s name, dosage forms, and other key information about the drug product.
PRINCIPAL DISPLAY PANEL Summer’s Eve Active Chafe Gel Dimethicone 1.2%/Skin Protectant Net Wt. 1.5 oz (42g) PRINCIPAL DISPLAY PANEL Summer’s Eve Active Chafe Gel Dimethicone 1.2%/Skin Protectant Net Wt. 1.5 oz (42g)

Spl unclassified section

Information not classified as belonging to one of the other fields. Approximately 40% of labeling with effective_time between June 2009 and August 2014 have information in this field.
Drug Facts

Do not use

Information about all contraindications for use. These contraindications are absolute and are intended for situations in which consumers should not use the product unless a prior diagnosis has been established by a doctor or for situations in which certain consumers should not use the product under any circumstances regardless of whether a doctor or health professional is consulted.
Do not use on deep or puncture wounds animal bites serious burns

Keep out of reach of children

Information pertaining to whether the product should be kept out of the reach of children, and instructions about what to do in the case of accidental contact or ingestion, if appropriate.
Keep out of reach of children . If swallowed get medical help or contact a Poison Control Center (1-800-222-1222) right away.

Other safety information

Information about safe use and handling of the product that may not have been specified in another field.
Other information Store at 20° – 25°C (68°-77°F)

Questions

A telephone number of a source to answer questions about a drug product. Sometimes available days and times are also noted.
Questions? 866 – 787 – 6383 or Summerseve.com

Stop use

Information about when use of the drug product should be discontinued immediately and a doctor consulted. Includes information about any signs of toxicity or other reactions that would necessitate immediately discontinuing use of the product.
Stop use and ask a doctor if condition worsens symptoms lasts more than 7 days or clear up and occur again within a few days

When using

Information about side effects that people may experience, and the substances (e.g. alcohol) or activities (e.g. operating machinery, driving a car) to avoid while using the drug product.
When using this product do not get into eyes

Warnings

Information about serious adverse reactions and potential safety hazards, including limitations in use imposed by those hazards and steps that should be taken if they occur.
Warnings For external use only . Do not use on deep or puncture wounds animal bites serious burns When using this product do not get into eyes Stop use and ask a doctor if condition worsens symptoms lasts more than 7 days or clear up and occur again within a few days Keep out of reach of children . If swallowed get medical help or contact a Poison Control Center (1-800-222-1222) right away.

Disclaimer: Do not rely on openFDA or Phanrmacy Near Me to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. Source: OpenFDA, Healthporta Drugs API