Label: DERMAZOR PSORIASIS AND SEBORRHEIC DERMATITIS- salicylic acid, zinc oxide cream
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Contains inactivated NDC Code(s)
NDC Code(s): 63302-202-01, 63302-202-02 - Packager: PRESTIGIO LTD
- 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 16, 2020
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- Active Ingredients
- Purpose
- Uses
- Warnings
- Directions
- Other Information
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Inactive Ingredients
anthemis nobilis flower oil, beeswax, bisabolol, borago officianalis seed oil, calamine, calendula officinalis flower oil, cannabis sativa seed oil, lanolin, lavandula angustifolia oil, linum usitatissimum seed oil, nigella sativa seed oil, oenothera biennis (evening primrose) oil, petrolatum, phenoxyetahnol,
polysorbate 80, prunus amygdalus dulcis (sweet almond) oil, retinyl palmitate (vitamin A), silybum marinum seed oil, sorbitan tristearate, tocopheryl
acetate (vitamin E), vitis vinifera (grape) seed oil, water, zea mays (corn) starch, zinc oxide. - Questions or Comments:
- SPL UNCLASSIFIED SECTION
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Principal Display Panel
NDC: 63302-202-02
DermaZor Psoriasis
MEDICATED SKIN TREATMENT
Psoriasis and Seborrheic Dermatitis Cream
Hypoallergenic No Side Effects
Relieves and helps prevent Symptomatic recurrences:
- Itching
- Irritation
- Redness
- Flaking
- Scaling
- Dryness
A Patented Unique Formula
3% Salicylic Acid, Zinc and Cannabis Oil Complex
Non-Steroidal, Non-Coal Tar
FL OZ | 100 ml 3.5
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INGREDIENTS AND APPEARANCE
DERMAZOR PSORIASIS AND SEBORRHEIC DERMATITIS
salicylic acid, zinc oxide creamProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:63302-202 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ) SALICYLIC ACID 3 g in 100 g Inactive Ingredients Ingredient Name Strength LANOLIN (UNII: 7EV65EAW6H) PETROLATUM (UNII: 4T6H12BN9U) WATER (UNII: 059QF0KO0R) ZINC OXIDE (UNII: SOI2LOH54Z) STARCH, CORN (UNII: O8232NY3SJ) GRAPE SEED OIL (UNII: 930MLC8XGG) CANNABIS SATIVA SEED OIL (UNII: 69VJ1LPN1S) CALENDULA OFFICINALIS FLOWER (UNII: P0M7O4Y7YD) CHAMAEMELUM NOBILE FLOWER OIL (UNII: UB27587839) EVENING PRIMROSE OIL (UNII: 3Q9L08K71N) WHITE WAX (UNII: 7G1J5DA97F) POLYSORBATE 65 (UNII: 14BGY2Y3MJ) POLYSORBATE 80 (UNII: 6OZP39ZG8H) SILYBUM MARIANUM SEED OIL (UNII: NYY23HEN06) PHENOXYETHANOL (UNII: HIE492ZZ3T) VITAMIN A (UNII: 81G40H8B0T) VITAMIN D (UNII: 9VU1KI44GP) BORAGE SEED OIL (UNII: F8XAG1755S) ALMOND OIL (UNII: 66YXD4DKO9) LEVOMENOL (UNII: 24WE03BX2T) NIGELLA SATIVA SEED OIL (UNII: CS4U38E731) LAVENDER OIL (UNII: ZBP1YXW0H8) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:63302-202-01 100 g in 1 TUBE; Type 0: Not a Combination Product 05/05/2014 2 NDC:63302-202-02 100 g in 1 TUBE; Type 0: Not a Combination Product 08/17/2017 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph final part358H 05/05/2014 Labeler - PRESTIGIO LTD (514838031) Registrant - PRESTIGIO LTD (514838031)