Label: CLINICIANS COMPLEX- sulfur lotion
- NDC Code(s): 72622-001-01
- Packager: SkinSx.com, Inc.
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: OTC monograph final
DISCLAIMER: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.
Drug Label Information
Updated January 14, 2022
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- Active Ingredients:
- Purpose
- Uses:
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Warnings:
For external use only • When using this product skin irritation and dryness is more likely to occur if you use another topical acne medication at the same time. If irritation occurs, only use one topical acne medication at a time • Do not use on broken skin or large areas of the skin • When using this product apply only to areas with acne. Avoid contact with eyes • If excessive irritation develops or increases, discontinue use and consult a doctor • Keep out of reach of children • If swallowed, get medical help or contact Poison Control Center right away.
- KEEP OUT OF REACH OF CHILDREN
- Directions:
- Inactive Ingredients:
- Other Information:
- Questions or Comments:
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
CLINICIANS COMPLEX
sulfur lotionProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:72622-001 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength SULFUR (UNII: 70FD1KFU70) (SULFUR - UNII:70FD1KFU70) SULFUR 100 mg in 1 g Inactive Ingredients Ingredient Name Strength ISOPROPYL ALCOHOL (UNII: ND2M416302) WATER (UNII: 059QF0KO0R) ZINC OXIDE (UNII: SOI2LOH54Z) CAMPHOR (SYNTHETIC) (UNII: 5TJD82A1ET) MAGNESIUM ALUMINUM SILICATE (UNII: 6M3P64V0NC) SALICYLIC ACID (UNII: O414PZ4LPZ) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:72622-001-01 31.0 g in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 11/01/2018 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph final part333D 11/01/2018 Labeler - SkinSx.com, Inc. (077455069) Establishment Name Address ID/FEI Business Operations A.I.G. Technologies, Inc. 086365223 manufacture(72622-001) , label(72622-001)