Label: SURIA RENEW INTENSIVE BODY lotion
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Contains inactivated NDC Code(s)
NDC Code(s): 81479-004-01 - Packager: SUN C&B
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: unapproved drug other
DISCLAIMER: This drug has not been found by FDA to be safe and effective, and this labeling has not been approved by FDA. For further information about unapproved drugs, click here.
Drug Label Information
Updated January 29, 2021
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- ACTIVE INGREDIENT
- INACTIVE INGREDIENT
- PURPOSE
- KEEP OUT OF REACH OF CHILDREN
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WARNINGS
1. If any of the following Symptoms occur, Cease use immediately. Continued usage would exacerbate the
symptoms. If symptoms persist, consult a doctor.
1) During of after usage, if red spots appear or you suffer from welling or itching or any other abnormal
symptoms after direct exposure to sunlight, consult a doctor immediately.
2)Avoid usage on cuts and wounds.
3) Storage and usage precautions.
A) Keep it out of reach of children.
B) Avoid exposure to direct sunlight during storage. - INDICATIONS & USAGE
- DOSAGE & ADMINISTRATION
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
SURIA RENEW INTENSIVE BODY
suria renew intensive body lotionProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:81479-004 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength METHYLPROPANEDIOL (UNII: N8F53B3R4R) (METHYLPROPANEDIOL - UNII:N8F53B3R4R) METHYLPROPANEDIOL 2 g in 200 mL GLYCERIN (UNII: PDC6A3C0OX) (GLYCERIN - UNII:PDC6A3C0OX) GLYCERIN 2 g in 200 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) 190 mL in 200 mL Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:81479-004-01 200 mL in 1 TUBE; Type 0: Not a Combination Product 01/01/2021 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 01/01/2021 Labeler - SUN C&B (695641205) Establishment Name Address ID/FEI Business Operations SUN C&B 695641205 manufacture(81479-004)
