Label: PETGLOW DERMAL GLAND- sulphur, chamomilla spray
- NDC Code(s): 83819-009-04
- Packager: Celcius Corp.
- Category: OTC ANIMAL DRUG LABEL
- DEA Schedule: None
- Marketing Status: unapproved homeopathic
DISCLAIMER: This drug has not been found by FDA to be safe and effective, and this labeling has not been approved by FDA. For further information about unapproved drugs, click here.
Drug Label Information
Updated January 10, 2024
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- Drug Facts
- Active ingredient
- Purpose
- Uses
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Warnings
For external Veterinary use only.
Do not use • If Anal Gland is severely swollen or significant swelling. Please consult a Vet
When using this product • Skin Inflammation and dryness is more likely to occur if you use another topical Gland medication at the same time, If irritation occurs, only use one topical Anal Gland medication at a time.
Stop use and ask a doctor if
• If symptoms persist or swelling increases after 10 days of use or if the infection visibly increases. -
Directions
• Spray our Natural solution directly on the affected anal area and gently massage to help soothen the skin. Use often atleast 3-4 times a day, often as needed or check with your Veterinarian. For best results it may take 2-3 weeks for the infection to subside. Alternatively you can also use the product on a cotton ball and gently apply.
- Other information
- Inactive ingredients
- Questions?
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SPL UNCLASSIFIED SECTION
PURE & NATURAL
NATURAL INGREDIENTS
ANTI-BACTERIAL ANAL GLAND MEDICINE
HOMEOPATHIC MEDICINE
PRESCRIPTION STRENGTH, COMPLETE ANAL GLAD SKIN HYGIENE
No Carcinogens
No Phthalates
No Parabens
No ChloridesDistributed by:
Celcius Corp
21415 Civic Center Dr
Southfield, MI 48034
sales@celcius.us
www.mypetglow.com - Packaging
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INGREDIENTS AND APPEARANCE
PETGLOW DERMAL GLAND
sulphur, chamomilla sprayProduct Information Product Type OTC ANIMAL DRUG Item Code (Source) NDC:83819-009 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength SULFUR (UNII: 70FD1KFU70) (SULFUR - UNII:70FD1KFU70) SULFUR 6 [hp_X] in 118 mL CHAMOMILE (UNII: FGL3685T2X) (CHAMOMILE - UNII:FGL3685T2X) CHAMOMILE 6 [hp_X] in 118 mL Inactive Ingredients Ingredient Name Strength AZADIRACHTA INDICA SEED OIL (UNII: 4DKJ9B3K2T) GLYCERIN (UNII: PDC6A3C0OX) LAVENDER OIL (UNII: ZBP1YXW0H8) OLIVE OIL (UNII: 6UYK2W1W1E) KARUM SEED OIL (UNII: 62160PU6FJ) CALAMUS OIL (UNII: 5F9K5X640P) TURMERIC (UNII: 856YO1Z64F) XANTHAN GUM (UNII: TTV12P4NEE) WATER (UNII: 059QF0KO0R) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:83819-009-04 118 mL in 1 BOTTLE, SPRAY Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved homeopathic 01/01/2024 Labeler - Celcius Corp. (117755609)