NDC 71607-100 Symba Skin Lightening
NDC Product Code 71607-100
Proprietary Name: Symba Skin Lightening 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.
Drug Use Information
Drug Use InformationThe drug use information is a summary and does NOT have all possible information about this product. This information does not assure that this product is safe, effective, or appropriate. This information is not individual medical advice and does not substitute for the advice of a health care professional. Always ask a health care professional for complete information about this product and your specific health needs.
- This product is used as skin lightening agent
Product Characteristics
Color(s):
WHITE (C48325)
NDC Code Structure
- 71607 - Craig Doura Llc
- 71607-100 - Symba Skin Lightening
NDC 71607-100-01
Package Description: 1 TUBE in 1 CARTON > 57 g in 1 TUBE (71607-100-57)
NDC Product Information
Symba Skin Lightening with NDC 71607-100 is product labeled by Craig Doura Llc. The product's dosage form is and is administered via form.
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.
- WATER (UNII: 059QF0KO0R)
- GLYCERYL 1-STEARATE (UNII: 258491E1RZ)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- MINERAL OIL (UNII: T5L8T28FGP)
- CETYL PALMITATE (UNII: 5ZA2S6B08X)
- ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)
- DIMETHICONE (UNII: 92RU3N3Y1O)
- SODIUM LAURYL SULFATE (UNII: 368GB5141J)
- ALLANTOIN (UNII: 344S277G0Z)
- SODIUM METABISULFITE (UNII: 4VON5FNS3C)
- ASCORBIC ACID (UNII: PQ6CK8PD0R)
- PROPYLPARABEN (UNII: Z8IX2SC1OH)
- EDETATE DISODIUM (UNII: 7FLD91C86K)
- D&C RED NO. 33 (UNII: 9DBA0SBB0L)
Product Labeler Information
What is the Labeler Name?Name of Company corresponding to the labeler code segment of the Product NDC.
Labeler Name: Craig Doura Llc
Labeler Code: 71607
Start Marketing Date: 09-01-2017 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: 12-31-2018 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 - INACTIVATED, the listing data was inactivated by the FDA. 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.
Symba Skin Lightening Product Label Images
Symba Skin Lightening 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
- Other
- Active Ingredients
- Purpose
- Uses
- Do Not Use
- When Using This Product
- Stop Use And Consult A Doctor If
- Otc - Pregnancy Or Breast Feeding
- Otc - Keep Out Of Reach Of Children
- Directions
- Inactive Ingredients
Other
Drug Facts
Active Ingredients
Hydroquinone 1.9%
Purpose
Skin Lightening Agent
Uses
Gradually lightens uneven and dark discoloration. Fades freckles, age, and liver spots. Moisturizes the skin. Leaves skin perfumed, soft, and smooth.For external use only
Do Not Use
- On irritated or broken skinon children under 12 years oldto prevent sunburnin combination with products containing Resorcinol, Phenol, or Salicylic Acid
When Using This Product
- Mild irritation or temporary skin darkening may occuravoid contact with eyesavoid unnecessary sun exposure
Stop Use And Consult A Doctor If
- Darkening persistsirritation becomes severe
Otc - Pregnancy Or Breast Feeding
If pregnant or breast feeding, consult a doctor before use.
Otc - Keep Out Of Reach Of Children
KEEP OUT OF REACH OF CHILDREN. If swallowed, call poison control or get medical attention immediately.
Directions
- For sensitive skin, test overnight on a small section of skin inside the elbow before useapply a thin layer to skin on affected areasuse sunscreen to prevent darkening from recurringuse twice daily for at least 6 weeks or as directed by doctor
Inactive Ingredients
Water (Aqua), Glyceryl Monostearate, Propylene Glycol, Mineral Oil (Paraffinum Liquidum), Cetyl Palmitate, Isopropyl Myristate, Dimethicone, Sodium Lauryl Sulphate, Allantoin, Fragrance (Parfum), Sodium Metabisulfite, Ascorbic Acid (Vitamin C), Propylparaben, Edetate Disodium, D & C Red No. 33 (CI 17200).
* Please review the disclaimer below.