Label: PURITON SKIN PROTECTANT HOMEOPATHIC- alumina, calcarea fluorica, calcarea silicata, magnesia sulphurica, silicea, sulphur, titanium metallicum, zincum metallicum spray
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Contains inactivated NDC Code(s)
NDC Code(s): 70796-002-04 - Packager: Kadesh, Inc.
- Category: HUMAN OTC DRUG LABEL
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 August 6, 2016
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- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- Drug Facts
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Active ingredient
Alumina 7X HPUS
Calcarea Fluorica 6X HPUS
Calcarea Silicata 5X HPUS
Magnesia Sulphurica 7X HPUS
Silicea 4X HPUS
Sulphur 4X HPUS
Titanium Metallicum 7X HPUS
Zincum Metallicum 8X HPUSThe letters HPUS indicate that this ingredients is officially included in the Homoeopathic pharmacopoeia of the United States.
- Purpose
- Uses
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Warnings
Do not Use • on broken skin • large areas of the skin
When using this product
• do not get into eyes • replace cap after using
• Use on mild to moderate eczema
Stop use and ask a doctor if • condition worsens • condition last more than 7 days or clear up and occur again within a few days
If pregnant or breast-feeding, ask a health professional before use.
- KEEP OUT OF REACH OF CHILDREN
- Directions
- Inactive ingredients
- Other information
- QUESTIONS
- SPL UNCLASSIFIED SECTION
- Packaging
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INGREDIENTS AND APPEARANCE
PURITON SKIN PROTECTANT HOMEOPATHIC
alumina, calcarea fluorica, calcarea silicata, magnesia sulphurica, silicea, sulphur, titanium metallicum, zincum metallicum sprayProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:70796-002 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ALUMINUM OXIDE (UNII: LMI26O6933) (ALUMINUM OXIDE - UNII:LMI26O6933) ALUMINUM OXIDE 7 [hp_X] in 118 mL CALCIUM FLUORIDE (UNII: O3B55K4YKI) (FLUORIDE ION - UNII:Q80VPU408O) CALCIUM FLUORIDE 6 [hp_X] in 118 mL CALCIUM SILICATE (UNII: S4255P4G5M) (CALCIUM CATION - UNII:2M83C4R6ZB) CALCIUM SILICATE 5 [hp_X] in 118 mL MAGNESIUM SULFATE HEPTAHYDRATE (UNII: SK47B8698T) (MAGNESIUM CATION - UNII:T6V3LHY838) MAGNESIUM SULFATE HEPTAHYDRATE 7 [hp_X] in 118 mL SILICON DIOXIDE (UNII: ETJ7Z6XBU4) (SILICON DIOXIDE - UNII:ETJ7Z6XBU4) SILICON DIOXIDE 4 [hp_X] in 118 mL SULFUR (UNII: 70FD1KFU70) (SULFUR - UNII:70FD1KFU70) SULFUR 4 [hp_X] in 118 mL TITANIUM (UNII: D1JT611TNE) (TITANIUM - UNII:D1JT611TNE) TITANIUM 7 [hp_X] in 118 mL ZINC (UNII: J41CSQ7QDS) (ZINC - UNII:J41CSQ7QDS) ZINC 8 [hp_X] in 118 mL Inactive Ingredients Ingredient Name Strength KAOLIN (UNII: 24H4NWX5CO) CEROUS OXALATE NONAHYDRATE (UNII: 0UV74P3R0J) IRON (UNII: E1UOL152H7) FERRIC CHLORIDE HEXAHYDRATE (UNII: 0I2XIN602U) FERROSOFERRIC PHOSPHATE (UNII: 91GQH8I5F7) POTASSIUM SILICATE (UNII: J86L1GUL6K) MAGNESIUM CHLORIDE (UNII: 02F3473H9O) SODIUM CHLORIDE (UNII: 451W47IQ8X) SODIUM NITRATE (UNII: 8M4L3H2ZVZ) PHOSPHORUS (UNII: 27YLU75U4W) WATER (UNII: 059QF0KO0R) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:70796-002-04 1 in 1 CARTON 10/01/2016 1 118 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved homeopathic 10/01/2016 Labeler - Kadesh, Inc. (080278274) Establishment Name Address ID/FEI Business Operations Kadesh, Inc. 080278274 manufacture(70796-002)
