Label: DR BERRYS MULTI-PURPOSE SULFUR CREME- sulfur cream
- NDC Code(s): 10893-440-04
- Packager: Nature's Innovation, Inc.
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: unapproved homeopathic
DISCLAIMER: This homeopathic product has not been evaluated by the Food and Drug Administration for safety or efficacy. FDA is not aware of scientific evidence to support homeopathy as effective.
Drug Label Information
Updated December 14, 2020
If you are a consumer or patient please visit this version.
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- Official Label (Printer Friendly)
- Drug Facts
- Active Ingredients:
- Purpose:
- Uses:
- Warnings:
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Directions:
Cleanse skin thoroughly before applying. Cover the affected skin area with creme once per day. If excessive drying of the skin or rash occurs,
reduce the application of creme or discontinue use. To speed relief, we recommend using Dr.Berry’s Sulfur Soap with Lavender. Some
individuals may be sensitive to sulfur or essential oils. Skin test for tolerability. If irritation or reaction occurs, discontinue use. - Inactive Ingredients:
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SPL UNCLASSIFIED SECTION
Est. 1892
Dr. Berry’s Multi-Purpose Sulfur Creme can be used to relieve symptoms of a variety of skin disorders including:
acne, seborrheic dermatitis, mite infestations, or tinea fungal infections. It inhibits the growth of bacteria, has anti-fungal properties and exfoliates the skin. Dryness may occur.Close jar tight after each use.
Questions? Comments? 1-866-371-2499
Mfd. by: Nature’s Innovation, Inc.
5317 Palmero Ct., Buford, GA 30518*These statements or claims are based upon traditional homeopathic practice. They have not been reviewed by the Food & Drug Administration. “X “is a homeopathic dilution.
- Packaging
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INGREDIENTS AND APPEARANCE
DR BERRYS MULTI-PURPOSE SULFUR CREME
sulfur creamProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:10893-440 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength SULFUR (UNII: 70FD1KFU70) (SULFUR - UNII:70FD1KFU70) SULFUR 1 [hp_X] in 120 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC) CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S) GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4) SUNFLOWER OIL (UNII: 3W1JG795YI) PHENOXYETHANOL (UNII: HIE492ZZ3T) POLYSORBATE 20 (UNII: 7T1F30V5YH) POTASSIUM SORBATE (UNII: 1VPU26JZZ4) SODIUM HYDROXIDE (UNII: 55X04QC32I) TEA TREE OIL (UNII: VIF565UC2G) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:10893-440-04 120 mL in 1 JAR; Type 0: Not a Combination Product 12/14/2020 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved homeopathic 12/14/2020 Labeler - Nature's Innovation, Inc. (602969854) Establishment Name Address ID/FEI Business Operations Nature's Innovation, Inc. 602969854 manufacture(10893-440)
