Label: CELLZYME ON-TOX- peppermint oil eucalyptus oil ferric oxide red cream
- NDC Code(s): 24765-111-01
- Packager: PHARMACAL-INTERNATIONAL. CO., LTD
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: OTC monograph not 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 May 20, 2021
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- Actvie Ingrdients
-
Inactives
WATER, PROPYLENE GLYCOL, HUMAN EMBRYONIC STEM CELL CONDITIONED MEDIA, MAGNESIUM ALUMINIUM SILICATE, DIMETHICONE/VINYL DIMETHICONE CROSSPOLYMER,HEXANEDIOL, SODIUM SILICATE, SLACTIC ACID, CAPRYLYL GLYCOL, ETHYLHEXYLGLYCERIN, XANTHAN GUM, ADENOSINE, DISODIUM EDTA, FRAGRANCE, SALIX ALBA (WILLOW) BARK EXTRACT, ORIGANUM VULGARE LEAF EXTRACT, SCUTELLARIA CAICALENSIS ROOT EXTRACT, CINNAMOMUM CASSIA BARK EXTRACT, LACTOBACILLUS/SOYBEAN FERMENT EXTRACT, PORTULACA OLERACEA EXTRACT, CHAMAECYPARIS OBTUSA LEAF EXTRACT, IRON OXIDES(CI77492)
- Purpose
- Indication and Usage
- Dosage and Administration
- Warnings
- KEEP OUT OF REACH OF CHILDREN
- Product Labels
-
INGREDIENTS AND APPEARANCE
CELLZYME ON-TOX
peppermint oil eucalyptus oil ferric oxide red creamProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:24765-111 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength PEPPERMINT OIL (UNII: AV092KU4JH) (PEPPERMINT - UNII:V95R5KMY2B) PEPPERMINT OIL 0.089 g in 100 g EUCALYPTUS OIL (UNII: 2R04ONI662) (EUCALYPTUS OIL - UNII:2R04ONI662) EUCALYPTUS OIL 0.092 g in 100 g FERRIC OXIDE RED (UNII: 1K09F3G675) (FERRIC OXIDE RED - UNII:1K09F3G675) FERRIC OXIDE RED 0.084 g in 100 g Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) PROPYLENE GLYCOL (UNII: 6DC9Q167V3) MAGNESIUM ALUMINUM SILICATE (UNII: 6M3P64V0NC) DIMETHICONE/VINYL DIMETHICONE CROSSPOLYMER (SOFT PARTICLE) (UNII: 9E4CO0W6C5) HEXANEDIOL (UNII: ZIA319275I) SODIUM SILICATE (UNII: IJF18F77L3) SALICYLIC ACID (UNII: O414PZ4LPZ) CAPRYLYL GLYCOL (UNII: 00YIU5438U) ETHYLHEXYLGLYCERIN (UNII: 147D247K3P) XANTHAN GUM (UNII: TTV12P4NEE) ADENOSINE (UNII: K72T3FS567) EDETATE DISODIUM ANHYDROUS (UNII: 8NLQ36F6MM) SALIX ALBA BARK (UNII: 205MXS71H7) OREGANO (UNII: 0E5AT8T16U) SCUTELLARIA BAICALENSIS ROOT (UNII: 7J95K7ID2S) CHINESE CINNAMON (UNII: WS4CQ062KM) SOYBEAN (UNII: L7HT8F1ZOD) PURSLANE (UNII: M6S840WXG5) CHAMAECYPARIS OBTUSA LEAF (UNII: 7OL154J5XB) FERRIC OXIDE YELLOW (UNII: EX438O2MRT) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:24765-111-01 5 g in 1 AMPULE; Type 0: Not a Combination Product 09/14/2017 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part356 08/16/2017 Labeler - PHARMACAL-INTERNATIONAL. CO., LTD (557805060)